Name: rs17423910
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs17423910

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:66223426 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.158540 (41964/264690, TOPMED)
G=0.196290 (42030/214122, ALFA)
G=0.158000 (22119/139994, GnomAD) (+ 20 more)
G=0.07768 (2195/28258, 14KJPN)
G=0.08007 (1342/16760, 8.3KJPN)
G=0.1483 (950/6404, 1000G_30x)
G=0.1480 (741/5008, 1000G)
G=0.1239 (555/4480, Estonian)
G=0.2055 (792/3854, ALSPAC)
G=0.2230 (827/3708, TWINSUK)
G=0.1006 (294/2922, KOREAN)
G=0.1536 (320/2084, HGDP_Stanford)
G=0.1379 (261/1892, HapMap)
G=0.2007 (228/1136, Daghestan)
G=0.213 (213/998, GoNL)
G=0.113 (71/626, Chileans)
G=0.187 (112/600, NorthernSweden)
G=0.236 (51/216, Qatari)
G=0.136 (29/214, Vietnamese)
A=0.434 (53/122, SGDP_PRJ)
G=0.22 (20/92, Ancient Sardinia)
G=0.10 (4/40, GENOME_DK)
A=0.4 (3/8, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PDE4B : Intron Variant
Publications: 1 citation
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	214212	A=0.803666	G=0.196334
European	Sub	184408	A=0.795746	G=0.204254
African	Sub	10408	A=0.90450	G=0.09550
African Others	Sub	360	A=0.933	G=0.067
African American	Sub	10048	A=0.90346	G=0.09654
Asian	Sub	752	A=0.878	G=0.122
East Asian	Sub	574	A=0.890	G=0.110
Other Asian	Sub	178	A=0.837	G=0.163
Latin American 1	Sub	928	A=0.831	G=0.169
Latin American 2	Sub	5000	A=0.8644	G=0.1356
South Asian	Sub	5054	A=0.7901	G=0.2099
Other	Sub	7662	A=0.8161	G=0.1839

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	A=0.841460	G=0.158540
Allele Frequency Aggregator	Total	Global	214122	A=0.803710	G=0.196290
Allele Frequency Aggregator	European	Sub	184334	A=0.795789	G=0.204211
Allele Frequency Aggregator	African	Sub	10408	A=0.90450	G=0.09550
Allele Frequency Aggregator	Other	Sub	7646	A=0.8162	G=0.1838
Allele Frequency Aggregator	South Asian	Sub	5054	A=0.7901	G=0.2099
Allele Frequency Aggregator	Latin American 2	Sub	5000	A=0.8644	G=0.1356
Allele Frequency Aggregator	Latin American 1	Sub	928	A=0.831	G=0.169
Allele Frequency Aggregator	Asian	Sub	752	A=0.878	G=0.122
gnomAD - Genomes	Global	Study-wide	139994	A=0.842000	G=0.158000
gnomAD - Genomes	European	Sub	75832	A=0.81252	G=0.18748
gnomAD - Genomes	African	Sub	41932	A=0.90186	G=0.09814
gnomAD - Genomes	American	Sub	13634	A=0.84803	G=0.15197
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	A=0.7146	G=0.2854
gnomAD - Genomes	East Asian	Sub	3124	A=0.8688	G=0.1312
gnomAD - Genomes	Other	Sub	2154	A=0.8338	G=0.1662
14KJPN	JAPANESE	Study-wide	28258	A=0.92232	G=0.07768
8.3KJPN	JAPANESE	Study-wide	16760	A=0.91993	G=0.08007
1000Genomes_30x	Global	Study-wide	6404	A=0.8517	G=0.1483
1000Genomes_30x	African	Sub	1786	A=0.9026	G=0.0974
1000Genomes_30x	Europe	Sub	1266	A=0.7844	G=0.2156
1000Genomes_30x	South Asian	Sub	1202	A=0.8453	G=0.1547
1000Genomes_30x	East Asian	Sub	1170	A=0.8538	G=0.1462
1000Genomes_30x	American	Sub	980	A=0.851	G=0.149
1000Genomes	Global	Study-wide	5008	A=0.8520	G=0.1480
1000Genomes	African	Sub	1322	A=0.9062	G=0.0938
1000Genomes	East Asian	Sub	1008	A=0.8591	G=0.1409
1000Genomes	Europe	Sub	1006	A=0.7833	G=0.2167
1000Genomes	South Asian	Sub	978	A=0.842	G=0.158
1000Genomes	American	Sub	694	A=0.853	G=0.147
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.8761	G=0.1239
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.7945	G=0.2055
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.7770	G=0.2230
KOREAN population from KRGDB	KOREAN	Study-wide	2922	A=0.8994	G=0.1006
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.8464	G=0.1536
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.900	G=0.100
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.751	G=0.249
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.811	G=0.189
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.797	G=0.203
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.905	G=0.095
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.931	G=0.069
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.99	G=0.01
HapMap	Global	Study-wide	1892	A=0.8621	G=0.1379
HapMap	American	Sub	770	A=0.821	G=0.179
HapMap	African	Sub	692	A=0.918	G=0.082
HapMap	Asian	Sub	254	A=0.913	G=0.087
HapMap	Europe	Sub	176	A=0.750	G=0.250
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	A=0.7993	G=0.2007
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	A=0.807	G=0.193
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.715	G=0.285
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	A=0.852	G=0.148
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.796	G=0.204
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	A=0.87	G=0.13
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.64	G=0.36
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.787	G=0.213
Chileans	Chilean	Study-wide	626	A=0.887	G=0.113
Northern Sweden	ACPOP	Study-wide	600	A=0.813	G=0.187
Qatari	Global	Study-wide	216	A=0.764	G=0.236
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.864	G=0.136
SGDP_PRJ	Global	Study-wide	122	A=0.434	G=0.566
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	92	A=0.78	G=0.22
The Danish reference pan genome	Danish	Study-wide	40	A=0.90	G=0.10
Siberian	Global	Study-wide	8	A=0.4	G=0.6

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.66223426A>G
GRCh37.p13 chr 1	NC_000001.10:g.66689109A>G
PDE4B RefSeqGene	NG_029038.1:g.435917A>G

Gene: PDE4B, phosphodiesterase 4B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PDE4B transcript variant c	NM_001037340.3:c.237-2403… NM_001037340.3:c.237-24034A>G	N/A	Intron Variant
PDE4B transcript variant d	NM_001037341.2:c.282-2403… NM_001037341.2:c.282-24034A>G	N/A	Intron Variant
PDE4B transcript variant e	NM_001297440.2:c.6-24034A… NM_001297440.2:c.6-24034A>G	N/A	Intron Variant
PDE4B transcript variant f	NM_001297441.1:c.57-24034… NM_001297441.1:c.57-24034A>G	N/A	Intron Variant
PDE4B transcript variant a	NM_002600.4:c.282-24034A>G	N/A	Intron Variant
PDE4B transcript variant b	NM_001037339.2:c.	N/A	Genic Upstream Transcript Variant
PDE4B transcript variant g	NM_001297442.2:c.	N/A	Genic Upstream Transcript Variant
PDE4B transcript variant X3	XM_005270924.4:c.	N/A	Genic Upstream Transcript Variant
PDE4B transcript variant X5	XM_005270925.3:c.	N/A	Genic Upstream Transcript Variant
PDE4B transcript variant X2	XM_006710680.4:c.	N/A	Genic Upstream Transcript Variant
PDE4B transcript variant X1	XM_017001445.2:c.	N/A	Genic Upstream Transcript Variant
PDE4B transcript variant X4	XM_047422401.1:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	A=	G
GRCh38.p14 chr 1	NC_000001.11:g.66223426=	NC_000001.11:g.66223426A>G
GRCh37.p13 chr 1	NC_000001.10:g.66689109=	NC_000001.10:g.66689109A>G
PDE4B RefSeqGene	NG_029038.1:g.435917=	NG_029038.1:g.435917A>G
PDE4B transcript variant c	NM_001037340.1:c.237-24034=	NM_001037340.1:c.237-24034A>G
PDE4B transcript variant c	NM_001037340.3:c.237-24034=	NM_001037340.3:c.237-24034A>G
PDE4B transcript variant d	NM_001037341.1:c.282-24034=	NM_001037341.1:c.282-24034A>G
PDE4B transcript variant d	NM_001037341.2:c.282-24034=	NM_001037341.2:c.282-24034A>G
PDE4B transcript variant e	NM_001297440.2:c.6-24034=	NM_001297440.2:c.6-24034A>G
PDE4B transcript variant f	NM_001297441.1:c.57-24034=	NM_001297441.1:c.57-24034A>G
PDE4B transcript variant a	NM_002600.3:c.282-24034=	NM_002600.3:c.282-24034A>G
PDE4B transcript variant a	NM_002600.4:c.282-24034=	NM_002600.4:c.282-24034A>G

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

123 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss24247677	Sep 20, 2004 (123)
2	ABI	ss28532810	Dec 02, 2004 (126)
3	AFFY	ss66476560	Dec 02, 2006 (127)
4	ILLUMINA	ss66832675	Dec 02, 2006 (127)
5	ILLUMINA	ss67185975	Dec 02, 2006 (127)
6	ILLUMINA	ss67560440	Dec 02, 2006 (127)
7	ILLUMINA	ss70664047	May 26, 2008 (130)
8	ILLUMINA	ss71225604	May 18, 2007 (127)
9	ILLUMINA	ss75894948	Dec 05, 2007 (129)
10	AFFY	ss76288524	Dec 05, 2007 (129)
11	ILLUMINA	ss79090995	Dec 15, 2007 (130)
12	KRIBB_YJKIM	ss85385744	Dec 15, 2007 (130)
13	HUMANGENOME_JCVI	ss99214390	Feb 06, 2009 (130)
14	BGI	ss102748647	Dec 01, 2009 (131)
15	1000GENOMES	ss110570401	Jan 25, 2009 (130)
16	ILLUMINA	ss121797114	Dec 01, 2009 (131)
17	ILLUMINA	ss153677078	Dec 01, 2009 (131)
18	GMI	ss155112218	Dec 01, 2009 (131)
19	ILLUMINA	ss159318121	Dec 01, 2009 (131)
20	ILLUMINA	ss160443106	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss163468459	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss164455356	Jul 04, 2010 (132)
23	ILLUMINA	ss170782342	Jul 04, 2010 (132)
24	ILLUMINA	ss172827289	Jul 04, 2010 (132)
25	AFFY	ss173137248	Jul 04, 2010 (132)
26	BUSHMAN	ss198560071	Jul 04, 2010 (132)
27	1000GENOMES	ss218428225	Jul 14, 2010 (132)
28	1000GENOMES	ss230566330	Jul 14, 2010 (132)
29	1000GENOMES	ss238254822	Jul 15, 2010 (132)
30	BL	ss253150920	May 09, 2011 (134)
31	GMI	ss275857589	May 04, 2012 (137)
32	ILLUMINA	ss480239110	May 04, 2012 (137)
33	ILLUMINA	ss480249818	May 04, 2012 (137)
34	ILLUMINA	ss480988529	Sep 08, 2015 (146)
35	ILLUMINA	ss484917524	May 04, 2012 (137)
36	ILLUMINA	ss536968523	Sep 08, 2015 (146)
37	TISHKOFF	ss554202008	Apr 25, 2013 (138)
38	SSMP	ss648072126	Apr 25, 2013 (138)
39	ILLUMINA	ss778834979	Sep 08, 2015 (146)
40	ILLUMINA	ss782905072	Sep 08, 2015 (146)
41	ILLUMINA	ss783868370	Sep 08, 2015 (146)
42	ILLUMINA	ss825421513	Jul 19, 2016 (147)
43	ILLUMINA	ss832159918	Sep 08, 2015 (146)
44	ILLUMINA	ss832830159	Jul 12, 2019 (153)
45	ILLUMINA	ss834295470	Sep 08, 2015 (146)
46	EVA-GONL	ss975242154	Aug 21, 2014 (142)
47	JMKIDD_LAB	ss1067949981	Aug 21, 2014 (142)
48	1000GENOMES	ss1291203456	Aug 21, 2014 (142)
49	HAMMER_LAB	ss1397248268	Sep 08, 2015 (146)
50	DDI	ss1425835608	Apr 01, 2015 (144)
51	EVA_GENOME_DK	ss1574117005	Apr 01, 2015 (144)
52	EVA_DECODE	ss1584611433	Apr 01, 2015 (144)
53	EVA_UK10K_ALSPAC	ss1600339457	Apr 01, 2015 (144)
54	EVA_UK10K_TWINSUK	ss1643333490	Apr 01, 2015 (144)
55	EVA_SVP	ss1712339773	Apr 01, 2015 (144)
56	ILLUMINA	ss1751929912	Sep 08, 2015 (146)
57	HAMMER_LAB	ss1794489838	Sep 08, 2015 (146)
58	WEILL_CORNELL_DGM	ss1918450203	Feb 12, 2016 (147)
59	GENOMED	ss1966765238	Jul 19, 2016 (147)
60	JJLAB	ss2019742311	Sep 14, 2016 (149)
61	USC_VALOUEV	ss2147758126	Dec 20, 2016 (150)
62	HUMAN_LONGEVITY	ss2163152634	Dec 20, 2016 (150)
63	ILLUMINA	ss2632526245	Nov 08, 2017 (151)
64	ILLUMINA	ss2634999255	Nov 08, 2017 (151)
65	GRF	ss2697675340	Nov 08, 2017 (151)
66	GNOMAD	ss2756026164	Nov 08, 2017 (151)
67	AFFY	ss2984861977	Nov 08, 2017 (151)
68	AFFY	ss2985515188	Nov 08, 2017 (151)
69	SWEGEN	ss2986941680	Nov 08, 2017 (151)
70	BIOINF_KMB_FNS_UNIBA	ss3023632714	Nov 08, 2017 (151)
71	CSHL	ss3343490590	Nov 08, 2017 (151)
72	ILLUMINA	ss3626116295	Oct 11, 2018 (152)
73	ILLUMINA	ss3630561864	Oct 11, 2018 (152)
74	ILLUMINA	ss3632894713	Oct 11, 2018 (152)
75	ILLUMINA	ss3633589418	Oct 11, 2018 (152)
76	ILLUMINA	ss3634328684	Oct 11, 2018 (152)
77	ILLUMINA	ss3635283217	Oct 11, 2018 (152)
78	ILLUMINA	ss3636005092	Oct 11, 2018 (152)
79	ILLUMINA	ss3637033643	Oct 11, 2018 (152)
80	ILLUMINA	ss3637761760	Oct 11, 2018 (152)
81	ILLUMINA	ss3638899805	Oct 11, 2018 (152)
82	ILLUMINA	ss3639447520	Oct 11, 2018 (152)
83	ILLUMINA	ss3640036045	Oct 11, 2018 (152)
84	ILLUMINA	ss3640982288	Oct 11, 2018 (152)
85	ILLUMINA	ss3641276252	Oct 11, 2018 (152)
86	ILLUMINA	ss3642773432	Oct 11, 2018 (152)
87	URBANLAB	ss3646680202	Oct 11, 2018 (152)
88	ILLUMINA	ss3653634742	Oct 11, 2018 (152)
89	EGCUT_WGS	ss3655011457	Jul 12, 2019 (153)
90	EVA_DECODE	ss3686925186	Jul 12, 2019 (153)
91	ACPOP	ss3727115347	Jul 12, 2019 (153)
92	ILLUMINA	ss3744629650	Jul 12, 2019 (153)
93	EVA	ss3746300899	Jul 12, 2019 (153)
94	ILLUMINA	ss3772130985	Jul 12, 2019 (153)
95	PACBIO	ss3783431660	Jul 12, 2019 (153)
96	PACBIO	ss3789086444	Jul 12, 2019 (153)
97	PACBIO	ss3793959222	Jul 12, 2019 (153)
98	KHV_HUMAN_GENOMES	ss3799307784	Jul 12, 2019 (153)
99	EVA	ss3826212346	Apr 25, 2020 (154)
100	EVA	ss3836493525	Apr 25, 2020 (154)
101	EVA	ss3841900041	Apr 25, 2020 (154)
102	HGDP	ss3847336309	Apr 25, 2020 (154)
103	SGDP_PRJ	ss3849010293	Apr 25, 2020 (154)
104	KRGDB	ss3894036956	Apr 25, 2020 (154)
105	EVA	ss3984801828	Apr 25, 2021 (155)
106	EVA	ss4016915023	Apr 25, 2021 (155)
107	TOPMED	ss4452478121	Apr 25, 2021 (155)
108	TOMMO_GENOMICS	ss5144298905	Apr 25, 2021 (155)
109	1000G_HIGH_COVERAGE	ss5242539622	Oct 12, 2022 (156)
110	EVA	ss5314621938	Oct 12, 2022 (156)
111	EVA	ss5319224435	Oct 12, 2022 (156)
112	HUGCELL_USP	ss5443575373	Oct 12, 2022 (156)
113	EVA	ss5505877861	Oct 12, 2022 (156)
114	1000G_HIGH_COVERAGE	ss5514951642	Oct 12, 2022 (156)
115	SANFORD_IMAGENETICS	ss5624207585	Oct 12, 2022 (156)
116	SANFORD_IMAGENETICS	ss5625684120	Oct 12, 2022 (156)
117	TOMMO_GENOMICS	ss5669170802	Oct 12, 2022 (156)
118	EVA	ss5799486627	Oct 12, 2022 (156)
119	YY_MCH	ss5800664324	Oct 12, 2022 (156)
120	EVA	ss5832064404	Oct 12, 2022 (156)
121	EVA	ss5848939611	Oct 12, 2022 (156)
122	EVA	ss5908572335	Oct 12, 2022 (156)
123	EVA	ss5937522042	Oct 12, 2022 (156)
124	1000Genomes	NC_000001.10 - 66689109	Oct 11, 2018 (152)
125	1000Genomes_30x	NC_000001.11 - 66223426	Oct 12, 2022 (156)
126	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 66689109	Oct 11, 2018 (152)
127	Chileans	NC_000001.10 - 66689109	Apr 25, 2020 (154)
128	Genome-wide autozygosity in Daghestan	NC_000001.9 - 66461697	Apr 25, 2020 (154)
129	Genetic variation in the Estonian population	NC_000001.10 - 66689109	Oct 11, 2018 (152)
130	The Danish reference pan genome	NC_000001.10 - 66689109	Apr 25, 2020 (154)
131	gnomAD - Genomes	NC_000001.11 - 66223426	Apr 25, 2021 (155)
132	Genome of the Netherlands Release 5	NC_000001.10 - 66689109	Apr 25, 2020 (154)
133	HGDP-CEPH-db Supplement 1	NC_000001.9 - 66461697	Apr 25, 2020 (154)
134	HapMap	NC_000001.11 - 66223426	Apr 25, 2020 (154)
135	KOREAN population from KRGDB	NC_000001.10 - 66689109	Apr 25, 2020 (154)
136	Northern Sweden	NC_000001.10 - 66689109	Jul 12, 2019 (153)
137	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 66689109	Apr 25, 2021 (155)
138	Qatari	NC_000001.10 - 66689109	Apr 25, 2020 (154)
139	SGDP_PRJ	NC_000001.10 - 66689109	Apr 25, 2020 (154)
140	Siberian	NC_000001.10 - 66689109	Apr 25, 2020 (154)
141	8.3KJPN	NC_000001.10 - 66689109	Apr 25, 2021 (155)
142	14KJPN	NC_000001.11 - 66223426	Oct 12, 2022 (156)
143	TopMed	NC_000001.11 - 66223426	Apr 25, 2021 (155)
144	UK 10K study - Twins	NC_000001.10 - 66689109	Oct 11, 2018 (152)
145	A Vietnamese Genetic Variation Database	NC_000001.10 - 66689109	Jul 12, 2019 (153)
146	ALFA	NC_000001.11 - 66223426	Apr 25, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs17878295	Mar 10, 2006 (126)
rs60494102	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3638899805, ss3639447520	NC_000001.8:66401129:A:G	NC_000001.11:66223425:A:G	(self)
9657, 14201, ss110570401, ss163468459, ss164455356, ss198560071, ss253150920, ss275857589, ss480239110, ss825421513, ss1397248268, ss1584611433, ss1712339773, ss2634999255, ss3642773432, ss3847336309	NC_000001.9:66461696:A:G	NC_000001.11:66223425:A:G	(self)
1932952, 1058405, 10795, 749705, 1534168, 451731, 1214350, 400212, 27755, 492133, 1027273, 274480, 2268212, 1058405, 221207, ss218428225, ss230566330, ss238254822, ss480249818, ss480988529, ss484917524, ss536968523, ss554202008, ss648072126, ss778834979, ss782905072, ss783868370, ss832159918, ss832830159, ss834295470, ss975242154, ss1067949981, ss1291203456, ss1425835608, ss1574117005, ss1600339457, ss1643333490, ss1751929912, ss1794489838, ss1918450203, ss1966765238, ss2019742311, ss2147758126, ss2632526245, ss2697675340, ss2756026164, ss2984861977, ss2985515188, ss2986941680, ss3343490590, ss3626116295, ss3630561864, ss3632894713, ss3633589418, ss3634328684, ss3635283217, ss3636005092, ss3637033643, ss3637761760, ss3640036045, ss3640982288, ss3641276252, ss3653634742, ss3655011457, ss3727115347, ss3744629650, ss3746300899, ss3772130985, ss3783431660, ss3789086444, ss3793959222, ss3826212346, ss3836493525, ss3849010293, ss3894036956, ss3984801828, ss4016915023, ss5144298905, ss5314621938, ss5319224435, ss5505877861, ss5624207585, ss5625684120, ss5799486627, ss5832064404, ss5937522042	NC_000001.10:66689108:A:G	NC_000001.11:66223425:A:G	(self)
2477577, 13634337, 86467, 3007906, 16084456, 15611652952, ss2163152634, ss3023632714, ss3646680202, ss3686925186, ss3799307784, ss3841900041, ss4452478121, ss5242539622, ss5443575373, ss5514951642, ss5669170802, ss5800664324, ss5848939611, ss5908572335	NC_000001.11:66223425:A:G	NC_000001.11:66223425:A:G	(self)
ss24247677, ss28532810, ss66476560, ss66832675, ss67185975, ss67560440, ss70664047, ss71225604, ss75894948, ss76288524, ss79090995, ss85385744, ss99214390, ss102748647, ss121797114, ss153677078, ss155112218, ss159318121, ss160443106, ss170782342, ss172827289, ss173137248	NT_032977.9:36661026:A:G	NC_000001.11:66223425:A:G	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs17423910

PMID	Title	Author	Year	Journal
25919455	Investigating the Role of Gene-Gene Interactions in TB Susceptibility.	Daya M et al.	2014	PloS one

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

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Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs17423910