Name: rs2297170
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.

rs2297170

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:100353717 (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: T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.193536 (51227/264690, TOPMED)
C=0.173737 (31886/183530, GnomAD_exome)
C=0.191676 (30892/161168, ALFA) (+ 21 more)
C=0.199872 (28006/140120, GnomAD)
C=0.19219 (10360/53904, ExAC)
C=0.10886 (3076/28256, 14KJPN)
C=0.10776 (1806/16760, 8.3KJPN)
C=0.20311 (2629/12944, GO-ESP)
C=0.1732 (1109/6404, 1000G_30x)
C=0.1705 (854/5008, 1000G)
C=0.2002 (897/4480, Estonian)
C=0.2109 (813/3854, ALSPAC)
C=0.1874 (695/3708, TWINSUK)
C=0.1328 (389/2930, KOREAN)
C=0.1952 (369/1890, HapMap)
C=0.214 (214/998, GoNL)
C=0.217 (130/600, NorthernSweden)
C=0.167 (89/534, MGP)
C=0.227 (49/216, Qatari)
C=0.132 (28/212, Vietnamese)
T=0.397 (69/174, SGDP_PRJ)
C=0.15 (6/40, GENOME_DK)
T=0.50 (7/14, Siberian)
C=0.50 (7/14, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: CDC14A : Intron Variant
Publications: 0 citations
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	161168	T=0.808324	C=0.191676
European	Sub	134790	T=0.805757	C=0.194243
African	Sub	9904	T=0.7878	C=0.2122
African Others	Sub	334	T=0.781	C=0.219
African American	Sub	9570	T=0.7880	C=0.2120
Asian	Sub	686	T=0.853	C=0.147
East Asian	Sub	524	T=0.861	C=0.139
Other Asian	Sub	162	T=0.827	C=0.173
Latin American 1	Sub	752	T=0.738	C=0.262
Latin American 2	Sub	6332	T=0.8861	C=0.1139
South Asian	Sub	184	T=0.891	C=0.109
Other	Sub	8520	T=0.8158	C=0.1842

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	T=0.806464	C=0.193536
gnomAD - Exomes	Global	Study-wide	183530	T=0.826263	C=0.173737
gnomAD - Exomes	European	Sub	94152	T=0.79560	C=0.20440
gnomAD - Exomes	Asian	Sub	37106	T=0.88697	C=0.11303
gnomAD - Exomes	American	Sub	26194	T=0.89005	C=0.10995
gnomAD - Exomes	African	Sub	12246	T=0.78230	C=0.21770
gnomAD - Exomes	Ashkenazi Jewish	Sub	8902	T=0.7745	C=0.2255
gnomAD - Exomes	Other	Sub	4930	T=0.8187	C=0.1813
Allele Frequency Aggregator	Total	Global	161168	T=0.808324	C=0.191676
Allele Frequency Aggregator	European	Sub	134790	T=0.805757	C=0.194243
Allele Frequency Aggregator	African	Sub	9904	T=0.7878	C=0.2122
Allele Frequency Aggregator	Other	Sub	8520	T=0.8158	C=0.1842
Allele Frequency Aggregator	Latin American 2	Sub	6332	T=0.8861	C=0.1139
Allele Frequency Aggregator	Latin American 1	Sub	752	T=0.738	C=0.262
Allele Frequency Aggregator	Asian	Sub	686	T=0.853	C=0.147
Allele Frequency Aggregator	South Asian	Sub	184	T=0.891	C=0.109
gnomAD - Genomes	Global	Study-wide	140120	T=0.800128	C=0.199872
gnomAD - Genomes	European	Sub	75886	T=0.80023	C=0.19977
gnomAD - Genomes	African	Sub	41980	T=0.78416	C=0.21584
gnomAD - Genomes	American	Sub	13652	T=0.83731	C=0.16269
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.7729	C=0.2271
gnomAD - Genomes	East Asian	Sub	3130	T=0.8764	C=0.1236
gnomAD - Genomes	Other	Sub	2148	T=0.8035	C=0.1965
ExAC	Global	Study-wide	53904	T=0.80781	C=0.19219
ExAC	Europe	Sub	28798	T=0.77151	C=0.22849
ExAC	Asian	Sub	15096	T=0.87931	C=0.12069
ExAC	African	Sub	6126	T=0.7677	C=0.2323
ExAC	American	Sub	3462	T=0.8674	C=0.1326
ExAC	Other	Sub	422	T=0.820	C=0.180
14KJPN	JAPANESE	Study-wide	28256	T=0.89114	C=0.10886
8.3KJPN	JAPANESE	Study-wide	16760	T=0.89224	C=0.10776
GO Exome Sequencing Project	Global	Study-wide	12944	T=0.79689	C=0.20311
GO Exome Sequencing Project	European American	Sub	8564	T=0.8034	C=0.1966
GO Exome Sequencing Project	African American	Sub	4380	T=0.7842	C=0.2158
1000Genomes_30x	Global	Study-wide	6404	T=0.8268	C=0.1732
1000Genomes_30x	African	Sub	1786	T=0.7682	C=0.2318
1000Genomes_30x	Europe	Sub	1266	T=0.7994	C=0.2006
1000Genomes_30x	South Asian	Sub	1202	T=0.8852	C=0.1148
1000Genomes_30x	East Asian	Sub	1170	T=0.8658	C=0.1342
1000Genomes_30x	American	Sub	980	T=0.851	C=0.149
1000Genomes	Global	Study-wide	5008	T=0.8295	C=0.1705
1000Genomes	African	Sub	1322	T=0.7716	C=0.2284
1000Genomes	East Asian	Sub	1008	T=0.8671	C=0.1329
1000Genomes	Europe	Sub	1006	T=0.7962	C=0.2038
1000Genomes	South Asian	Sub	978	T=0.887	C=0.113
1000Genomes	American	Sub	694	T=0.853	C=0.147
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.7998	C=0.2002
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.7891	C=0.2109
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8126	C=0.1874
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.8672	C=0.1328
HapMap	Global	Study-wide	1890	T=0.8048	C=0.1952
HapMap	American	Sub	770	T=0.839	C=0.161
HapMap	African	Sub	692	T=0.756	C=0.244
HapMap	Asian	Sub	252	T=0.849	C=0.151
HapMap	Europe	Sub	176	T=0.784	C=0.216
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.786	C=0.214
Northern Sweden	ACPOP	Study-wide	600	T=0.783	C=0.217
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.833	C=0.167
Qatari	Global	Study-wide	216	T=0.773	C=0.227
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.868	C=0.132
SGDP_PRJ	Global	Study-wide	174	T=0.397	C=0.603
The Danish reference pan genome	Danish	Study-wide	40	T=0.85	C=0.15
Siberian	Global	Study-wide	14	T=0.50	C=0.50

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.100353717T>C
GRCh37.p13 chr 1	NC_000001.10:g.100819273T>C
CDC14A RefSeqGene (LRG_1418)	NG_051602.2:g.13717T>C

Gene: CDC14A, cell division cycle 14A (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CDC14A transcript variant 4	NM_001319210.2:c.50-45T>C	N/A	Intron Variant
CDC14A transcript variant 5	NM_001319211.2:c.-125-45T… NM_001319211.2:c.-125-45T>C	N/A	Intron Variant
CDC14A transcript variant 6	NM_001319212.2:c.-742-45T… NM_001319212.2:c.-742-45T>C	N/A	Intron Variant
CDC14A transcript variant 1	NM_003672.4:c.50-45T>C	N/A	Intron Variant
CDC14A transcript variant 2	NM_033312.3:c.50-45T>C	N/A	Intron Variant
CDC14A transcript variant 3	NM_033313.3:c.50-45T>C	N/A	Intron 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.

Allele: C (allele ID: 656814 )

ClinVar Accession	Disease Names	Clinical Significance
RCV000843112.1	not provided	Benign

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	T=	C
GRCh38.p14 chr 1	NC_000001.11:g.100353717=	NC_000001.11:g.100353717T>C
GRCh37.p13 chr 1	NC_000001.10:g.100819273=	NC_000001.10:g.100819273T>C
CDC14A RefSeqGene (LRG_1418)	NG_051602.2:g.13717=	NG_051602.2:g.13717T>C
CDC14A transcript variant 4	NM_001319210.2:c.50-45=	NM_001319210.2:c.50-45T>C
CDC14A transcript variant 5	NM_001319211.2:c.-125-45=	NM_001319211.2:c.-125-45T>C
CDC14A transcript variant 6	NM_001319212.2:c.-742-45=	NM_001319212.2:c.-742-45T>C
CDC14A transcript variant 1	NM_003672.3:c.50-45=	NM_003672.3:c.50-45T>C
CDC14A transcript variant 1	NM_003672.4:c.50-45=	NM_003672.4:c.50-45T>C
CDC14A transcript variant 2	NM_033312.2:c.50-45=	NM_033312.2:c.50-45T>C
CDC14A transcript variant 2	NM_033312.3:c.50-45=	NM_033312.3:c.50-45T>C
CDC14A transcript variant 3	NM_033313.2:c.50-45=	NM_033313.2:c.50-45T>C
CDC14A transcript variant 3	NM_033313.3:c.50-45=	NM_033313.3:c.50-45T>C
CDC14A transcript variant X1	XM_005271294.1:c.53-45=	XM_005271294.1:c.53-45T>C
CDC14A transcript variant X2	XM_005271295.1:c.50-45=	XM_005271295.1:c.50-45T>C
CDC14A transcript variant X3	XM_005271296.1:c.53-45=	XM_005271296.1:c.53-45T>C
CDC14A transcript variant X4	XM_005271297.1:c.-125-45=	XM_005271297.1:c.-125-45T>C

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#.

107 SubSNP, 23 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss3241505	Sep 28, 2001 (100)
2	PERLEGEN	ss23162341	Sep 20, 2004 (123)
3	EGP_SNPS	ss35035692	May 24, 2005 (125)
4	ILLUMINA	ss65750226	Oct 15, 2006 (127)
5	EGP_SNPS	ss66862690	Nov 30, 2006 (127)
6	PERLEGEN	ss68775546	May 17, 2007 (127)
7	ILLUMINA	ss75015848	Dec 06, 2007 (129)
8	SI_EXO	ss76884597	Dec 06, 2007 (129)
9	BGI	ss102768240	Dec 01, 2009 (131)
10	ILLUMINA-UK	ss118922547	Feb 14, 2009 (130)
11	KRIBB_YJKIM	ss119429371	Dec 01, 2009 (131)
12	ILLUMINA	ss160532352	Dec 01, 2009 (131)
13	ILLUMINA	ss173268768	Jul 04, 2010 (132)
14	BUSHMAN	ss198838383	Jul 04, 2010 (132)
15	1000GENOMES	ss218551488	Jul 14, 2010 (132)
16	1000GENOMES	ss230658787	Jul 14, 2010 (132)
17	1000GENOMES	ss238325147	Jul 15, 2010 (132)
18	GMI	ss275946974	May 04, 2012 (137)
19	ILLUMINA	ss480518727	May 04, 2012 (137)
20	ILLUMINA	ss480533125	May 04, 2012 (137)
21	ILLUMINA	ss481343872	Sep 08, 2015 (146)
22	ILLUMINA	ss485056712	May 04, 2012 (137)
23	1000GENOMES	ss489754274	May 04, 2012 (137)
24	ILLUMINA	ss537073351	Sep 08, 2015 (146)
25	TISHKOFF	ss554485505	Apr 25, 2013 (138)
26	SSMP	ss648257309	Apr 25, 2013 (138)
27	NHLBI-ESP	ss712319964	Apr 25, 2013 (138)
28	ILLUMINA	ss778491076	Aug 21, 2014 (142)
29	ILLUMINA	ss782974571	Sep 08, 2015 (146)
30	ILLUMINA	ss783935847	Aug 21, 2014 (142)
31	ILLUMINA	ss832230951	Sep 08, 2015 (146)
32	ILLUMINA	ss833947080	Aug 21, 2014 (142)
33	EVA-GONL	ss975488812	Aug 21, 2014 (142)
34	JMKIDD_LAB	ss1068131298	Aug 21, 2014 (142)
35	1000GENOMES	ss1292127111	Aug 21, 2014 (142)
36	DDI	ss1425912565	Apr 01, 2015 (144)
37	EVA_GENOME_DK	ss1574274940	Apr 01, 2015 (144)
38	EVA_DECODE	ss1584866820	Apr 01, 2015 (144)
39	EVA_UK10K_ALSPAC	ss1600827731	Apr 01, 2015 (144)
40	EVA_UK10K_TWINSUK	ss1643821764	Apr 01, 2015 (144)
41	EVA_EXAC	ss1685656487	Apr 01, 2015 (144)
42	EVA_MGP	ss1710913579	Apr 01, 2015 (144)
43	EVA_SVP	ss1712357565	Apr 01, 2015 (144)
44	ILLUMINA	ss1751859478	Sep 08, 2015 (146)
45	HAMMER_LAB	ss1794814802	Sep 08, 2015 (146)
46	WEILL_CORNELL_DGM	ss1918687778	Feb 12, 2016 (147)
47	GENOMED	ss1966821810	Jul 19, 2016 (147)
48	JJLAB	ss2019865781	Sep 14, 2016 (149)
49	USC_VALOUEV	ss2147884285	Dec 20, 2016 (150)
50	HUMAN_LONGEVITY	ss2165073420	Dec 20, 2016 (150)
51	ILLUMINA	ss2632554186	Nov 08, 2017 (151)
52	GRF	ss2697811484	Nov 08, 2017 (151)
53	GNOMAD	ss2731666888	Nov 08, 2017 (151)
54	GNOMAD	ss2746381264	Nov 08, 2017 (151)
55	GNOMAD	ss2758695313	Nov 08, 2017 (151)
56	SWEGEN	ss2987313897	Nov 08, 2017 (151)
57	BIOINF_KMB_FNS_UNIBA	ss3023696131	Nov 08, 2017 (151)
58	CSHL	ss3343597986	Nov 08, 2017 (151)
59	ILLUMINA	ss3626166488	Oct 11, 2018 (152)
60	ILLUMINA	ss3630588330	Oct 11, 2018 (152)
61	ILLUMINA	ss3632903478	Oct 11, 2018 (152)
62	ILLUMINA	ss3633598481	Oct 11, 2018 (152)
63	ILLUMINA	ss3634339601	Oct 11, 2018 (152)
64	ILLUMINA	ss3635292088	Oct 11, 2018 (152)
65	ILLUMINA	ss3636017104	Oct 11, 2018 (152)
66	ILLUMINA	ss3637042546	Oct 11, 2018 (152)
67	ILLUMINA	ss3637775787	Oct 11, 2018 (152)
68	ILLUMINA	ss3640046961	Oct 11, 2018 (152)
69	ILLUMINA	ss3640984567	Oct 11, 2018 (152)
70	ILLUMINA	ss3641278556	Oct 11, 2018 (152)
71	ILLUMINA	ss3642785958	Oct 11, 2018 (152)
72	OMUKHERJEE_ADBS	ss3646233805	Oct 11, 2018 (152)
73	EGCUT_WGS	ss3655399573	Jul 12, 2019 (153)
74	EVA_DECODE	ss3687377333	Jul 12, 2019 (153)
75	ACPOP	ss3727318796	Jul 12, 2019 (153)
76	ILLUMINA	ss3744640570	Jul 12, 2019 (153)
77	EVA	ss3746579828	Jul 12, 2019 (153)
78	ILLUMINA	ss3772141803	Jul 12, 2019 (153)
79	KHV_HUMAN_GENOMES	ss3799580658	Jul 12, 2019 (153)
80	EVA	ss3823634847	Apr 25, 2020 (154)
81	EVA	ss3825570324	Apr 25, 2020 (154)
82	EVA	ss3826329410	Apr 25, 2020 (154)
83	SGDP_PRJ	ss3849487766	Apr 25, 2020 (154)
84	KRGDB	ss3894567029	Apr 25, 2020 (154)
85	FSA-LAB	ss3983938626	Apr 25, 2021 (155)
86	FSA-LAB	ss3983938627	Apr 25, 2021 (155)
87	EVA	ss3986128934	Apr 25, 2021 (155)
88	EVA	ss4016927987	Apr 25, 2021 (155)
89	TOPMED	ss4460878320	Apr 25, 2021 (155)
90	TOMMO_GENOMICS	ss5145336139	Apr 25, 2021 (155)
91	1000G_HIGH_COVERAGE	ss5243338735	Oct 12, 2022 (156)
92	EVA	ss5314638434	Oct 12, 2022 (156)
93	EVA	ss5320704299	Oct 12, 2022 (156)
94	HUGCELL_USP	ss5444289957	Oct 12, 2022 (156)
95	1000G_HIGH_COVERAGE	ss5516189905	Oct 12, 2022 (156)
96	EVA	ss5623994956	Oct 12, 2022 (156)
97	SANFORD_IMAGENETICS	ss5626141585	Oct 12, 2022 (156)
98	TOMMO_GENOMICS	ss5670502363	Oct 12, 2022 (156)
99	EVA	ss5799493714	Oct 12, 2022 (156)
100	EVA	ss5800083524	Oct 12, 2022 (156)
101	YY_MCH	ss5800863975	Oct 12, 2022 (156)
102	EVA	ss5832379061	Oct 12, 2022 (156)
103	EVA	ss5848266340	Oct 12, 2022 (156)
104	EVA	ss5849035571	Oct 12, 2022 (156)
105	EVA	ss5909493352	Oct 12, 2022 (156)
106	EVA	ss5938003284	Oct 12, 2022 (156)
107	EVA	ss5979974123	Oct 12, 2022 (156)
108	1000Genomes	NC_000001.10 - 100819273	Oct 11, 2018 (152)
109	1000Genomes_30x	NC_000001.11 - 100353717	Oct 12, 2022 (156)
110	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 100819273	Oct 11, 2018 (152)
111	Genetic variation in the Estonian population	NC_000001.10 - 100819273	Oct 11, 2018 (152)
112	ExAC	NC_000001.10 - 100819273	Oct 11, 2018 (152)
113	The Danish reference pan genome	NC_000001.10 - 100819273	Apr 25, 2020 (154)
114	gnomAD - Genomes	NC_000001.11 - 100353717	Apr 25, 2021 (155)
115	gnomAD - Exomes	NC_000001.10 - 100819273	Jul 12, 2019 (153)
116	GO Exome Sequencing Project	NC_000001.10 - 100819273	Oct 11, 2018 (152)
117	Genome of the Netherlands Release 5	NC_000001.10 - 100819273	Apr 25, 2020 (154)
118	HapMap	NC_000001.11 - 100353717	Apr 25, 2020 (154)
119	KOREAN population from KRGDB	NC_000001.10 - 100819273	Apr 25, 2020 (154)
120	Medical Genome Project healthy controls from Spanish population	NC_000001.10 - 100819273	Apr 25, 2020 (154)
121	Northern Sweden	NC_000001.10 - 100819273	Jul 12, 2019 (153)
122	Qatari	NC_000001.10 - 100819273	Apr 25, 2020 (154)
123	SGDP_PRJ	NC_000001.10 - 100819273	Apr 25, 2020 (154)
124	Siberian	NC_000001.10 - 100819273	Apr 25, 2020 (154)
125	8.3KJPN	NC_000001.10 - 100819273	Apr 25, 2021 (155)
126	14KJPN	NC_000001.11 - 100353717	Oct 12, 2022 (156)
127	TopMed	NC_000001.11 - 100353717	Apr 25, 2021 (155)
128	UK 10K study - Twins	NC_000001.10 - 100819273	Oct 11, 2018 (152)
129	A Vietnamese Genetic Variation Database	NC_000001.10 - 100819273	Jul 12, 2019 (153)
130	ALFA	NC_000001.11 - 100353717	Apr 25, 2021 (155)
131	ClinVar	RCV000843112.1	Apr 25, 2020 (154)

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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss118922547, ss160532352, ss198838383, ss275946974, ss480518727, ss1584866820, ss1712357565, ss3642785958	NC_000001.9:100591860:T:C	NC_000001.11:100353716:T:C	(self)
2891539, 1595895, 1137821, 4863121, 1630918, 689004, 93478, 692738, 1744423, 30331, 603661, 729708, 1504746, 400639, 3305446, 1595895, 343619, ss218551488, ss230658787, ss238325147, ss480533125, ss481343872, ss485056712, ss489754274, ss537073351, ss554485505, ss648257309, ss712319964, ss778491076, ss782974571, ss783935847, ss832230951, ss833947080, ss975488812, ss1068131298, ss1292127111, ss1425912565, ss1574274940, ss1600827731, ss1643821764, ss1685656487, ss1710913579, ss1751859478, ss1794814802, ss1918687778, ss1966821810, ss2019865781, ss2147884285, ss2632554186, ss2697811484, ss2731666888, ss2746381264, ss2758695313, ss2987313897, ss3343597986, ss3626166488, ss3630588330, ss3632903478, ss3633598481, ss3634339601, ss3635292088, ss3636017104, ss3637042546, ss3637775787, ss3640046961, ss3640984567, ss3641278556, ss3646233805, ss3655399573, ss3727318796, ss3744640570, ss3746579828, ss3772141803, ss3823634847, ss3825570324, ss3826329410, ss3849487766, ss3894567029, ss3983938626, ss3983938627, ss3986128934, ss4016927987, ss5145336139, ss5314638434, ss5320704299, ss5623994956, ss5626141585, ss5799493714, ss5800083524, ss5832379061, ss5848266340, ss5938003284, ss5979974123	NC_000001.10:100819272:T:C	NC_000001.11:100353716:T:C	(self)
RCV000843112.1, 3715840, 20444925, 137694, 4339467, 24484655, 413666077, ss2165073420, ss3023696131, ss3687377333, ss3799580658, ss4460878320, ss5243338735, ss5444289957, ss5516189905, ss5670502363, ss5800863975, ss5849035571, ss5909493352	NC_000001.11:100353716:T:C	NC_000001.11:100353716:T:C	(self)
ss76884597	NT_032977.8:70791191:T:C	NC_000001.11:100353716:T:C	(self)
ss3241505, ss23162341, ss35035692, ss65750226, ss66862690, ss68775546, ss75015848, ss102768240, ss119429371, ss173268768	NT_032977.9:70791190:T:C	NC_000001.11:100353716:T:C	(self)

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

No publications for rs2297170

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

rs2297170