Name: rs720324
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.

rs720324

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:21400134 (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: C>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.398251 (105413/264690, TOPMED)
C=0.388167 (54324/139950, GnomAD)
C=0.27132 (7667/28258, 14KJPN) (+ 15 more)
C=0.27458 (4602/16760, 8.3KJPN)
C=0.4596 (4479/9746, ALFA)
C=0.4010 (2568/6404, 1000G_30x)
C=0.3944 (1975/5008, 1000G)
C=0.3487 (1562/4480, Estonian)
C=0.3433 (1323/3854, ALSPAC)
C=0.3174 (1177/3708, TWINSUK)
C=0.3147 (922/2930, KOREAN)
C=0.362 (361/998, GoNL)
C=0.345 (207/600, NorthernSweden)
C=0.270 (124/460, SGDP_PRJ)
C=0.333 (72/216, Qatari)
C=0.368 (78/212, Vietnamese)
C=0.37 (19/52, Siberian)
C=0.35 (14/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC105372558 : Non Coding Transcript 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	9746	C=0.4596	A=0.5404, T=0.0000
European	Sub	8084	C=0.4050	A=0.5950, T=0.0000
African	Sub	1208	C=0.7401	A=0.2599, T=0.0000
African Others	Sub	44	C=0.68	A=0.32, T=0.00
African American	Sub	1164	C=0.7423	A=0.2577, T=0.0000
Asian	Sub	10	C=0.9	A=0.1, T=0.0
East Asian	Sub	8	C=0.9	A=0.1, T=0.0
Other Asian	Sub	2	C=1.0	A=0.0, T=0.0
Latin American 1	Sub	14	C=1.00	A=0.00, T=0.00
Latin American 2	Sub	128	C=1.000	A=0.000, T=0.000
South Asian	Sub	12	C=0.83	A=0.17, T=0.00
Other	Sub	290	C=0.517	A=0.483, T=0.000

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	C=0.398251	A=0.601749
gnomAD - Genomes	Global	Study-wide	139950	C=0.388167	A=0.611833
gnomAD - Genomes	European	Sub	75838	C=0.33365	A=0.66635
gnomAD - Genomes	African	Sub	41890	C=0.50413	A=0.49587
gnomAD - Genomes	American	Sub	13626	C=0.38815	A=0.61185
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.2031	A=0.7969
gnomAD - Genomes	East Asian	Sub	3124	C=0.3537	A=0.6463
gnomAD - Genomes	Other	Sub	2148	C=0.3883	A=0.6117
14KJPN	JAPANESE	Study-wide	28258	C=0.27132	A=0.72868
8.3KJPN	JAPANESE	Study-wide	16760	C=0.27458	A=0.72542
Allele Frequency Aggregator	Total	Global	9746	C=0.4596	A=0.5404, T=0.0000
Allele Frequency Aggregator	European	Sub	8084	C=0.4050	A=0.5950, T=0.0000
Allele Frequency Aggregator	African	Sub	1208	C=0.7401	A=0.2599, T=0.0000
Allele Frequency Aggregator	Other	Sub	290	C=0.517	A=0.483, T=0.000
Allele Frequency Aggregator	Latin American 2	Sub	128	C=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	Latin American 1	Sub	14	C=1.00	A=0.00, T=0.00
Allele Frequency Aggregator	South Asian	Sub	12	C=0.83	A=0.17, T=0.00
Allele Frequency Aggregator	Asian	Sub	10	C=0.9	A=0.1, T=0.0
1000Genomes_30x	Global	Study-wide	6404	C=0.4010	A=0.5990
1000Genomes_30x	African	Sub	1786	C=0.5358	A=0.4642
1000Genomes_30x	Europe	Sub	1266	C=0.3349	A=0.6651
1000Genomes_30x	South Asian	Sub	1202	C=0.3087	A=0.6913
1000Genomes_30x	East Asian	Sub	1170	C=0.3282	A=0.6718
1000Genomes_30x	American	Sub	980	C=0.441	A=0.559
1000Genomes	Global	Study-wide	5008	C=0.3944	A=0.6056
1000Genomes	African	Sub	1322	C=0.5303	A=0.4697
1000Genomes	East Asian	Sub	1008	C=0.3383	A=0.6617
1000Genomes	Europe	Sub	1006	C=0.3300	A=0.6700
1000Genomes	South Asian	Sub	978	C=0.306	A=0.694
1000Genomes	American	Sub	694	C=0.435	A=0.565
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.3487	A=0.6513
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.3433	A=0.6567
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.3174	A=0.6826
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.3147	A=0.6853, G=0.0000, T=0.0000
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.362	A=0.638
Northern Sweden	ACPOP	Study-wide	600	C=0.345	A=0.655
SGDP_PRJ	Global	Study-wide	460	C=0.270	A=0.730
Qatari	Global	Study-wide	216	C=0.333	A=0.667
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.368	A=0.632
Siberian	Global	Study-wide	52	C=0.37	A=0.63
The Danish reference pan genome	Danish	Study-wide	40	C=0.35	A=0.65

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 20	NC_000020.11:g.21400134C>A
GRCh38.p14 chr 20	NC_000020.11:g.21400134C>G
GRCh38.p14 chr 20	NC_000020.11:g.21400134C>T
GRCh37.p13 chr 20	NC_000020.10:g.21380772C>A
GRCh37.p13 chr 20	NC_000020.10:g.21380772C>G
GRCh37.p13 chr 20	NC_000020.10:g.21380772C>T

Gene: LOC105372558, uncharacterized LOC105372558 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105372558 transcript variant X5	XR_007067725.1:n.694C>A	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X5	XR_007067725.1:n.694C>G	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X5	XR_007067725.1:n.694C>T	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X6	XR_937325.4:n.1097C>A	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X6	XR_937325.4:n.1097C>G	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X6	XR_937325.4:n.1097C>T	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X7	XR_001754527.3:n.1565C>A	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X7	XR_001754527.3:n.1565C>G	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X7	XR_001754527.3:n.1565C>T	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X8	XR_001754531.3:n.1189C>A	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X8	XR_001754531.3:n.1189C>G	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X8	XR_001754531.3:n.1189C>T	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X9	XR_937329.4:n.1427C>A	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X9	XR_937329.4:n.1427C>G	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X9	XR_937329.4:n.1427C>T	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X10	XR_937330.4:n.1055C>A	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X10	XR_937330.4:n.1055C>G	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X10	XR_937330.4:n.1055C>T	N/A	Non Coding Transcript Variant
LOC105372558 transcript variant X1	XR_001754526.1:n.	N/A	Intron Variant
LOC105372558 transcript variant X2	XR_001754528.1:n.	N/A	Intron Variant
LOC105372558 transcript variant X3	XR_001754530.1:n.	N/A	Intron Variant
LOC105372558 transcript variant X4	XR_001754532.1:n.	N/A	Genic Downstream 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	C=	A	G	T
GRCh38.p14 chr 20	NC_000020.11:g.21400134=	NC_000020.11:g.21400134C>A	NC_000020.11:g.21400134C>G	NC_000020.11:g.21400134C>T
GRCh37.p13 chr 20	NC_000020.10:g.21380772=	NC_000020.10:g.21380772C>A	NC_000020.10:g.21380772C>G	NC_000020.10:g.21380772C>T
LOC105372558 transcript variant X9	XR_937329.4:n.1427=	XR_937329.4:n.1427C>A	XR_937329.4:n.1427C>G	XR_937329.4:n.1427C>T
LOC105372558 transcript variant X9	XR_937329.3:n.953=	XR_937329.3:n.953C>A	XR_937329.3:n.953C>G	XR_937329.3:n.953C>T
LOC105372558 transcript variant X9	XR_937329.2:n.953=	XR_937329.2:n.953C>A	XR_937329.2:n.953C>G	XR_937329.2:n.953C>T
LOC105372558 transcript variant X6	XR_937325.4:n.1097=	XR_937325.4:n.1097C>A	XR_937325.4:n.1097C>G	XR_937325.4:n.1097C>T
LOC105372558 transcript variant X8	XR_937325.3:n.1097=	XR_937325.3:n.1097C>A	XR_937325.3:n.1097C>G	XR_937325.3:n.1097C>T
LOC105372558 transcript variant X8	XR_937325.2:n.1097=	XR_937325.2:n.1097C>A	XR_937325.2:n.1097C>G	XR_937325.2:n.1097C>T
LOC105372558 transcript variant X10	XR_937330.4:n.1055=	XR_937330.4:n.1055C>A	XR_937330.4:n.1055C>G	XR_937330.4:n.1055C>T
LOC105372558 transcript variant X10	XR_937330.3:n.1064=	XR_937330.3:n.1064C>A	XR_937330.3:n.1064C>G	XR_937330.3:n.1064C>T
LOC105372558 transcript variant X10	XR_937330.2:n.1064=	XR_937330.2:n.1064C>A	XR_937330.2:n.1064C>G	XR_937330.2:n.1064C>T
LOC105372558 transcript variant X7	XR_001754527.3:n.1565=	XR_001754527.3:n.1565C>A	XR_001754527.3:n.1565C>G	XR_001754527.3:n.1565C>T
LOC105372558 transcript variant X2	XR_001754527.2:n.1565=	XR_001754527.2:n.1565C>A	XR_001754527.2:n.1565C>G	XR_001754527.2:n.1565C>T
LOC105372558 transcript variant X2	XR_001754527.1:n.1565=	XR_001754527.1:n.1565C>A	XR_001754527.1:n.1565C>G	XR_001754527.1:n.1565C>T
LOC105372558 transcript variant X8	XR_001754531.3:n.1189=	XR_001754531.3:n.1189C>A	XR_001754531.3:n.1189C>G	XR_001754531.3:n.1189C>T
LOC105372558 transcript variant X6	XR_001754531.2:n.1189=	XR_001754531.2:n.1189C>A	XR_001754531.2:n.1189C>G	XR_001754531.2:n.1189C>T
LOC105372558 transcript variant X6	XR_001754531.1:n.1189=	XR_001754531.1:n.1189C>A	XR_001754531.1:n.1189C>G	XR_001754531.1:n.1189C>T
LOC105372558 transcript variant X5	XR_007067725.1:n.694=	XR_007067725.1:n.694C>A	XR_007067725.1:n.694C>G	XR_007067725.1:n.694C>T

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#.

79 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss61260	Oct 05, 2000 (86)
2	YUSUKE	ss4973874	Aug 28, 2002 (108)
3	SC_JCM	ss5697935	Feb 20, 2003 (111)
4	SC_SNP	ss8358597	Apr 21, 2003 (114)
5	BCM_SSAHASNP	ss10963437	Jul 11, 2003 (116)
6	WI_SSAHASNP	ss12490629	Jul 11, 2003 (116)
7	CSHL-HAPMAP	ss19477989	Feb 27, 2004 (120)
8	SSAHASNP	ss21782423	Apr 05, 2004 (123)
9	SEQUENOM	ss24793873	Sep 20, 2004 (123)
10	ABI	ss41407448	Mar 15, 2006 (126)
11	SI_EXO	ss52081591	Oct 15, 2006 (127)
12	BCMHGSC_JDW	ss91665909	Mar 24, 2008 (129)
13	HUMANGENOME_JCVI	ss96222107	Feb 06, 2009 (130)
14	1000GENOMES	ss111856725	Jan 25, 2009 (130)
15	1000GENOMES	ss113197314	Jan 25, 2009 (130)
16	ILLUMINA-UK	ss117511874	Feb 14, 2009 (130)
17	ENSEMBL	ss135744084	Dec 01, 2009 (131)
18	ENSEMBL	ss138223427	Dec 01, 2009 (131)
19	GMI	ss156265577	Dec 01, 2009 (131)
20	COMPLETE_GENOMICS	ss167977149	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss169326085	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss171995984	Jul 04, 2010 (132)
23	BUSHMAN	ss203856029	Jul 04, 2010 (132)
24	BCM-HGSC-SUB	ss208600916	Jul 04, 2010 (132)
25	1000GENOMES	ss228301928	Jul 14, 2010 (132)
26	1000GENOMES	ss237796988	Jul 15, 2010 (132)
27	1000GENOMES	ss243976234	Jul 15, 2010 (132)
28	BL	ss255539235	May 09, 2011 (134)
29	GMI	ss283332317	May 04, 2012 (137)
30	GMI	ss287437231	Apr 25, 2013 (138)
31	PJP	ss292629862	May 09, 2011 (134)
32	TISHKOFF	ss566188461	Apr 25, 2013 (138)
33	SSMP	ss662063605	Apr 25, 2013 (138)
34	EVA-GONL	ss994626055	Aug 21, 2014 (142)
35	JMKIDD_LAB	ss1082138104	Aug 21, 2014 (142)
36	1000GENOMES	ss1364380419	Aug 21, 2014 (142)
37	DDI	ss1429021788	Apr 01, 2015 (144)
38	EVA_GENOME_DK	ss1579472542	Apr 01, 2015 (144)
39	EVA_UK10K_ALSPAC	ss1638585213	Apr 01, 2015 (144)
40	EVA_UK10K_TWINSUK	ss1681579246	Apr 01, 2015 (144)
41	EVA_DECODE	ss1698684939	Apr 01, 2015 (144)
42	HAMMER_LAB	ss1809459107	Sep 08, 2015 (146)
43	WEILL_CORNELL_DGM	ss1938133009	Feb 12, 2016 (147)
44	JJLAB	ss2029851768	Sep 14, 2016 (149)
45	USC_VALOUEV	ss2158404592	Dec 20, 2016 (150)
46	HUMAN_LONGEVITY	ss2241985052	Dec 20, 2016 (150)
47	SYSTEMSBIOZJU	ss2629421133	Nov 08, 2017 (151)
48	GRF	ss2704080560	Nov 08, 2017 (151)
49	GNOMAD	ss2966314584	Nov 08, 2017 (151)
50	SWEGEN	ss3017995286	Nov 08, 2017 (151)
51	BIOINF_KMB_FNS_UNIBA	ss3028759160	Nov 08, 2017 (151)
52	CSHL	ss3352458195	Nov 08, 2017 (151)
53	URBANLAB	ss3650989672	Oct 12, 2018 (152)
54	EGCUT_WGS	ss3684720369	Jul 13, 2019 (153)
55	EVA_DECODE	ss3706717443	Jul 13, 2019 (153)
56	ACPOP	ss3743319924	Jul 13, 2019 (153)
57	EVA	ss3758524275	Jul 13, 2019 (153)
58	PACBIO	ss3788621374	Jul 13, 2019 (153)
59	PACBIO	ss3793518548	Jul 13, 2019 (153)
60	PACBIO	ss3798405727	Jul 13, 2019 (153)
61	KHV_HUMAN_GENOMES	ss3821692724	Jul 13, 2019 (153)
62	EVA	ss3835629960	Apr 27, 2020 (154)
63	EVA	ss3841441222	Apr 27, 2020 (154)
64	EVA	ss3846949356	Apr 27, 2020 (154)
65	SGDP_PRJ	ss3888897740	Apr 27, 2020 (154)
66	KRGDB	ss3939102679	Apr 27, 2020 (154)
67	TOPMED	ss5085023598	Apr 26, 2021 (155)
68	TOMMO_GENOMICS	ss5229192532	Apr 26, 2021 (155)
69	1000G_HIGH_COVERAGE	ss5308358180	Oct 13, 2022 (156)
70	HUGCELL_USP	ss5500736120	Oct 13, 2022 (156)
71	EVA	ss5512182996	Oct 13, 2022 (156)
72	1000G_HIGH_COVERAGE	ss5614579391	Oct 13, 2022 (156)
73	SANFORD_IMAGENETICS	ss5663022439	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5788278937	Oct 13, 2022 (156)
75	YY_MCH	ss5817886678	Oct 13, 2022 (156)
76	EVA	ss5845555628	Oct 13, 2022 (156)
77	EVA	ss5853104170	Oct 13, 2022 (156)
78	EVA	ss5922995014	Oct 13, 2022 (156)
79	EVA	ss5957936524	Oct 13, 2022 (156)
80	1000Genomes	NC_000020.10 - 21380772	Oct 12, 2018 (152)
81	1000Genomes_30x	NC_000020.11 - 21400134	Oct 13, 2022 (156)
82	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 21380772	Oct 12, 2018 (152)
83	Genetic variation in the Estonian population	NC_000020.10 - 21380772	Oct 12, 2018 (152)
84	The Danish reference pan genome	NC_000020.10 - 21380772	Apr 27, 2020 (154)
85	gnomAD - Genomes	NC_000020.11 - 21400134	Apr 26, 2021 (155)
86	Genome of the Netherlands Release 5	NC_000020.10 - 21380772	Apr 27, 2020 (154)
87	KOREAN population from KRGDB	NC_000020.10 - 21380772	Apr 27, 2020 (154)
88	Northern Sweden	NC_000020.10 - 21380772	Jul 13, 2019 (153)
89	Qatari	NC_000020.10 - 21380772	Apr 27, 2020 (154)
90	SGDP_PRJ	NC_000020.10 - 21380772	Apr 27, 2020 (154)
91	Siberian	NC_000020.10 - 21380772	Apr 27, 2020 (154)
92	8.3KJPN	NC_000020.10 - 21380772	Apr 26, 2021 (155)
93	14KJPN	NC_000020.11 - 21400134	Oct 13, 2022 (156)
94	TopMed	NC_000020.11 - 21400134	Apr 26, 2021 (155)
95	UK 10K study - Twins	NC_000020.10 - 21380772	Oct 12, 2018 (152)
96	A Vietnamese Genetic Variation Database	NC_000020.10 - 21380772	Jul 13, 2019 (153)
97	ALFA	NC_000020.11 - 21400134	Apr 26, 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)
rs3787505	Oct 08, 2002 (108)
rs13041651	Oct 07, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss91665909, ss111856725, ss113197314, ss117511874, ss167977149, ss169326085, ss171995984, ss203856029, ss208600916, ss255539235, ss283332317, ss287437231, ss292629862, ss1698684939	NC_000020.9:21328771:C:A	NC_000020.11:21400133:C:A	(self)
77831097, 43094258, 30458617, 5637481, 19202566, 46280073, 16604789, 20174931, 40914720, 10920946, 87161839, 43094258, 9516224, ss228301928, ss237796988, ss243976234, ss566188461, ss662063605, ss994626055, ss1082138104, ss1364380419, ss1429021788, ss1579472542, ss1638585213, ss1681579246, ss1809459107, ss1938133009, ss2029851768, ss2158404592, ss2629421133, ss2704080560, ss2966314584, ss3017995286, ss3352458195, ss3684720369, ss3743319924, ss3758524275, ss3788621374, ss3793518548, ss3798405727, ss3835629960, ss3841441222, ss3888897740, ss3939102679, ss5229192532, ss5512182996, ss5663022439, ss5845555628, ss5957936524	NC_000020.10:21380771:C:A	NC_000020.11:21400133:C:A	(self)
102105326, 548731228, 122116041, 360132543, 11400858950, ss2241985052, ss3028759160, ss3650989672, ss3706717443, ss3821692724, ss3846949356, ss5085023598, ss5308358180, ss5500736120, ss5614579391, ss5788278937, ss5817886678, ss5853104170, ss5922995014	NC_000020.11:21400133:C:A	NC_000020.11:21400133:C:A	(self)
ss61260, ss4973874, ss5697935, ss8358597, ss10963437, ss12490629, ss19477989, ss21782423, ss24793873, ss41407448, ss52081591, ss96222107, ss135744084, ss138223427, ss156265577	NT_011387.8:21320771:C:A	NC_000020.11:21400133:C:A	(self)
46280073, ss3939102679	NC_000020.10:21380771:C:G	NC_000020.11:21400133:C:G	(self)
46280073, ss3939102679	NC_000020.10:21380771:C:T	NC_000020.11:21400133:C:T	(self)
11400858950	NC_000020.11:21400133:C:T	NC_000020.11:21400133:C:T	(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 rs720324

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

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
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.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs720324