Name: rs7550402
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.

rs7550402

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:155755107 (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 / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.488133 (129204/264690, TOPMED)
C=0.467904 (61666/131792, GnomAD)
T=0.24944 (6948/27854, 14KJPN) (+ 14 more)
T=0.25060 (4163/16612, 8.3KJPN)
C=0.38995 (6162/15802, ALFA)
T=0.4408 (2823/6404, 1000G_30x)
T=0.4481 (2244/5008, 1000G)
C=0.2922 (1304/4462, Estonian)
C=0.3391 (1307/3854, ALSPAC)
C=0.3395 (1259/3708, TWINSUK)
T=0.2193 (642/2928, KOREAN)
C=0.371 (370/998, GoNL)
C=0.380 (228/600, NorthernSweden)
T=0.250 (100/400, SGDP_PRJ)
C=0.389 (84/216, Qatari)
C=0.38 (15/40, GENOME_DK)
T=0.28 (11/40, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GON4L : 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	15802	T=0.61005	C=0.38995, G=0.00000
European	Sub	11798	T=0.68537	C=0.31463, G=0.00000
African	Sub	2384	T=0.3003	C=0.6997, G=0.0000
African Others	Sub	86	T=0.17	C=0.83, G=0.00
African American	Sub	2298	T=0.3050	C=0.6950, G=0.0000
Asian	Sub	108	T=0.278	C=0.722, G=0.000
East Asian	Sub	84	T=0.27	C=0.73, G=0.00
Other Asian	Sub	24	T=0.29	C=0.71, G=0.00
Latin American 1	Sub	146	T=0.541	C=0.459, G=0.000
Latin American 2	Sub	610	T=0.511	C=0.489, G=0.000
South Asian	Sub	94	T=0.63	C=0.37, G=0.00
Other	Sub	662	T=0.541	C=0.459, G=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.511867	C=0.488133
gnomAD - Genomes	Global	Study-wide	131792	T=0.532096	C=0.467904
gnomAD - Genomes	European	Sub	72554	T=0.64997	C=0.35003
gnomAD - Genomes	African	Sub	38396	T=0.28844	C=0.71156
gnomAD - Genomes	American	Sub	12664	T=0.59563	C=0.40437
gnomAD - Genomes	Ashkenazi Jewish	Sub	3228	T=0.7221	C=0.2779
gnomAD - Genomes	East Asian	Sub	2952	T=0.3154	C=0.6846
gnomAD - Genomes	Other	Sub	1998	T=0.5445	C=0.4555
14KJPN	JAPANESE	Study-wide	27854	T=0.24944	C=0.75056
8.3KJPN	JAPANESE	Study-wide	16612	T=0.25060	C=0.74940
Allele Frequency Aggregator	Total	Global	15802	T=0.61005	C=0.38995, G=0.00000
Allele Frequency Aggregator	European	Sub	11798	T=0.68537	C=0.31463, G=0.00000
Allele Frequency Aggregator	African	Sub	2384	T=0.3003	C=0.6997, G=0.0000
Allele Frequency Aggregator	Other	Sub	662	T=0.541	C=0.459, G=0.000
Allele Frequency Aggregator	Latin American 2	Sub	610	T=0.511	C=0.489, G=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	T=0.541	C=0.459, G=0.000
Allele Frequency Aggregator	Asian	Sub	108	T=0.278	C=0.722, G=0.000
Allele Frequency Aggregator	South Asian	Sub	94	T=0.63	C=0.37, G=0.00
1000Genomes_30x	Global	Study-wide	6404	T=0.4408	C=0.5592
1000Genomes_30x	African	Sub	1786	T=0.1753	C=0.8247
1000Genomes_30x	Europe	Sub	1266	T=0.6351	C=0.3649
1000Genomes_30x	South Asian	Sub	1202	T=0.6165	C=0.3835
1000Genomes_30x	East Asian	Sub	1170	T=0.3128	C=0.6872
1000Genomes_30x	American	Sub	980	T=0.611	C=0.389
1000Genomes	Global	Study-wide	5008	T=0.4481	C=0.5519
1000Genomes	African	Sub	1322	T=0.1891	C=0.8109
1000Genomes	East Asian	Sub	1008	T=0.3155	C=0.6845
1000Genomes	Europe	Sub	1006	T=0.6461	C=0.3539
1000Genomes	South Asian	Sub	978	T=0.622	C=0.378
1000Genomes	American	Sub	694	T=0.602	C=0.398
Genetic variation in the Estonian population	Estonian	Study-wide	4462	T=0.7078	C=0.2922
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6609	C=0.3391
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.6605	C=0.3395
KOREAN population from KRGDB	KOREAN	Study-wide	2928	T=0.2193	C=0.7807, G=0.0000
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.629	C=0.371
Northern Sweden	ACPOP	Study-wide	600	T=0.620	C=0.380
SGDP_PRJ	Global	Study-wide	400	T=0.250	C=0.750
Qatari	Global	Study-wide	216	T=0.611	C=0.389
The Danish reference pan genome	Danish	Study-wide	40	T=0.62	C=0.38
Siberian	Global	Study-wide	40	T=0.28	C=0.72

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.155755107T>C
GRCh38.p14 chr 1	NC_000001.11:g.155755107T>G
GRCh37.p13 chr 1	NC_000001.10:g.155724898T>C
GRCh37.p13 chr 1	NC_000001.10:g.155724898T>G

Gene: GON4L, gon-4 like (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GON4L transcript variant 4	NM_001282856.2:c.5518-619… NM_001282856.2:c.5518-619A>G	N/A	Intron Variant
GON4L transcript variant 5	NM_001282858.2:c.5518-619… NM_001282858.2:c.5518-619A>G	N/A	Intron Variant
GON4L transcript variant 3	NM_001282860.2:c.5518-619… NM_001282860.2:c.5518-619A>G	N/A	Intron Variant
GON4L transcript variant 6	NM_001282861.2:c.	N/A	Genic Downstream Transcript Variant
GON4L transcript variant 2	NM_032292.6:c.	N/A	Genic Downstream Transcript Variant
GON4L transcript variant X9	XM_005245284.4:c.5002-619… XM_005245284.4:c.5002-619A>G	N/A	Intron Variant
GON4L transcript variant X16	XM_005245286.4:c.3106-619… XM_005245286.4:c.3106-619A>G	N/A	Intron Variant
GON4L transcript variant X3	XM_006711393.4:c.5518-619… XM_006711393.4:c.5518-619A>G	N/A	Intron Variant
GON4L transcript variant X4	XM_006711394.5:c.5518-619… XM_006711394.5:c.5518-619A>G	N/A	Intron Variant
GON4L transcript variant X1	XM_047423263.1:c.5518-619… XM_047423263.1:c.5518-619A>G	N/A	Intron Variant
GON4L transcript variant X2	XM_047423264.1:c.5518-619… XM_047423264.1:c.5518-619A>G	N/A	Intron Variant
GON4L transcript variant X5	XM_047423277.1:c.5518-619… XM_047423277.1:c.5518-619A>G	N/A	Intron Variant
GON4L transcript variant X6	XM_047423282.1:c.5431-619… XM_047423282.1:c.5431-619A>G	N/A	Intron Variant
GON4L transcript variant X7	XM_047423284.1:c.5431-619… XM_047423284.1:c.5431-619A>G	N/A	Intron Variant
GON4L transcript variant X8	XM_047423291.1:c.5431-619… XM_047423291.1:c.5431-619A>G	N/A	Intron Variant
GON4L transcript variant X10	XM_047423296.1:c.5002-619… XM_047423296.1:c.5002-619A>G	N/A	Intron Variant
GON4L transcript variant X11	XM_047423297.1:c.3808-619… XM_047423297.1:c.3808-619A>G	N/A	Intron Variant
GON4L transcript variant X12	XM_047423298.1:c.3808-619… XM_047423298.1:c.3808-619A>G	N/A	Intron Variant
GON4L transcript variant X13	XM_047423299.1:c.3808-619… XM_047423299.1:c.3808-619A>G	N/A	Intron Variant
GON4L transcript variant X14	XM_047423301.1:c.3721-619… XM_047423301.1:c.3721-619A>G	N/A	Intron Variant
GON4L transcript variant X15	XM_047423307.1:c.	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	T=	C	G
GRCh38.p14 chr 1	NC_000001.11:g.155755107=	NC_000001.11:g.155755107T>C	NC_000001.11:g.155755107T>G
GRCh37.p13 chr 1	NC_000001.10:g.155724898=	NC_000001.10:g.155724898T>C	NC_000001.10:g.155724898T>G
GON4L transcript variant 1	NM_001037533.1:c.5518-619=	NM_001037533.1:c.5518-619A>G	NM_001037533.1:c.5518-619A>C
GON4L transcript variant 4	NM_001282856.2:c.5518-619=	NM_001282856.2:c.5518-619A>G	NM_001282856.2:c.5518-619A>C
GON4L transcript variant 5	NM_001282858.2:c.5518-619=	NM_001282858.2:c.5518-619A>G	NM_001282858.2:c.5518-619A>C
GON4L transcript variant 3	NM_001282860.2:c.5518-619=	NM_001282860.2:c.5518-619A>G	NM_001282860.2:c.5518-619A>C
GON4L transcript variant X1	XM_005245277.1:c.5518-619=	XM_005245277.1:c.5518-619A>G	XM_005245277.1:c.5518-619A>C
GON4L transcript variant X2	XM_005245278.1:c.5518-619=	XM_005245278.1:c.5518-619A>G	XM_005245278.1:c.5518-619A>C
GON4L transcript variant X3	XM_005245279.1:c.5518-619=	XM_005245279.1:c.5518-619A>G	XM_005245279.1:c.5518-619A>C
GON4L transcript variant X4	XM_005245280.1:c.5518-619=	XM_005245280.1:c.5518-619A>G	XM_005245280.1:c.5518-619A>C
GON4L transcript variant X5	XM_005245281.1:c.5518-619=	XM_005245281.1:c.5518-619A>G	XM_005245281.1:c.5518-619A>C
GON4L transcript variant X6	XM_005245282.1:c.5518-619=	XM_005245282.1:c.5518-619A>G	XM_005245282.1:c.5518-619A>C
GON4L transcript variant X7	XM_005245283.1:c.5431-619=	XM_005245283.1:c.5431-619A>G	XM_005245283.1:c.5431-619A>C
GON4L transcript variant X8	XM_005245284.1:c.5002-619=	XM_005245284.1:c.5002-619A>G	XM_005245284.1:c.5002-619A>C
GON4L transcript variant X9	XM_005245284.4:c.5002-619=	XM_005245284.4:c.5002-619A>G	XM_005245284.4:c.5002-619A>C
GON4L transcript variant X10	XM_005245286.1:c.3106-619=	XM_005245286.1:c.3106-619A>G	XM_005245286.1:c.3106-619A>C
GON4L transcript variant X16	XM_005245286.4:c.3106-619=	XM_005245286.4:c.3106-619A>G	XM_005245286.4:c.3106-619A>C
GON4L transcript variant X3	XM_006711393.4:c.5518-619=	XM_006711393.4:c.5518-619A>G	XM_006711393.4:c.5518-619A>C
GON4L transcript variant X4	XM_006711394.5:c.5518-619=	XM_006711394.5:c.5518-619A>G	XM_006711394.5:c.5518-619A>C
GON4L transcript variant X1	XM_047423263.1:c.5518-619=	XM_047423263.1:c.5518-619A>G	XM_047423263.1:c.5518-619A>C
GON4L transcript variant X2	XM_047423264.1:c.5518-619=	XM_047423264.1:c.5518-619A>G	XM_047423264.1:c.5518-619A>C
GON4L transcript variant X5	XM_047423277.1:c.5518-619=	XM_047423277.1:c.5518-619A>G	XM_047423277.1:c.5518-619A>C
GON4L transcript variant X6	XM_047423282.1:c.5431-619=	XM_047423282.1:c.5431-619A>G	XM_047423282.1:c.5431-619A>C
GON4L transcript variant X7	XM_047423284.1:c.5431-619=	XM_047423284.1:c.5431-619A>G	XM_047423284.1:c.5431-619A>C
GON4L transcript variant X8	XM_047423291.1:c.5431-619=	XM_047423291.1:c.5431-619A>G	XM_047423291.1:c.5431-619A>C
GON4L transcript variant X10	XM_047423296.1:c.5002-619=	XM_047423296.1:c.5002-619A>G	XM_047423296.1:c.5002-619A>C
GON4L transcript variant X11	XM_047423297.1:c.3808-619=	XM_047423297.1:c.3808-619A>G	XM_047423297.1:c.3808-619A>C
GON4L transcript variant X12	XM_047423298.1:c.3808-619=	XM_047423298.1:c.3808-619A>G	XM_047423298.1:c.3808-619A>C
GON4L transcript variant X13	XM_047423299.1:c.3808-619=	XM_047423299.1:c.3808-619A>G	XM_047423299.1:c.3808-619A>C
GON4L transcript variant X14	XM_047423301.1:c.3721-619=	XM_047423301.1:c.3721-619A>G	XM_047423301.1:c.3721-619A>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#.

59 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss11419527	Jul 11, 2003 (116)
2	SC_SNP	ss13008659	Dec 05, 2003 (119)
3	SSAHASNP	ss20491881	Apr 05, 2004 (121)
4	ABI	ss41268299	Mar 14, 2006 (126)
5	HGSV	ss80823437	Dec 15, 2007 (130)
6	HUMANGENOME_JCVI	ss99251605	Feb 05, 2009 (130)
7	BGI	ss102786208	Dec 01, 2009 (131)
8	ENSEMBL	ss131696243	Dec 01, 2009 (131)
9	COMPLETE_GENOMICS	ss164133265	Jul 04, 2010 (132)
10	COMPLETE_GENOMICS	ss165230412	Jul 04, 2010 (132)
11	BUSHMAN	ss199093890	Jul 04, 2010 (132)
12	BCM-HGSC-SUB	ss205448804	Jul 04, 2010 (132)
13	GMI	ss276053176	May 04, 2012 (137)
14	PJP	ss290638154	May 09, 2011 (134)
15	1000GENOMES	ss328954995	May 09, 2011 (134)
16	TISHKOFF	ss554706119	Apr 25, 2013 (138)
17	SSMP	ss648418077	Apr 25, 2013 (138)
18	EVA-GONL	ss975689421	Aug 21, 2014 (142)
19	1000GENOMES	ss1292954808	Aug 21, 2014 (142)
20	EVA_GENOME_DK	ss1574395333	Apr 01, 2015 (144)
21	EVA_DECODE	ss1585071186	Apr 01, 2015 (144)
22	EVA_UK10K_ALSPAC	ss1601228758	Apr 01, 2015 (144)
23	EVA_UK10K_TWINSUK	ss1644222791	Apr 01, 2015 (144)
24	HAMMER_LAB	ss1795100627	Sep 08, 2015 (146)
25	WEILL_CORNELL_DGM	ss1918923083	Feb 12, 2016 (147)
26	JJLAB	ss2019976650	Sep 14, 2016 (149)
27	USC_VALOUEV	ss2148001890	Dec 20, 2016 (150)
28	SYSTEMSBIOZJU	ss2624496207	Nov 08, 2017 (151)
29	GRF	ss2697974623	Nov 08, 2017 (151)
30	GNOMAD	ss2761407948	Nov 08, 2017 (151)
31	SWEGEN	ss2987764397	Nov 08, 2017 (151)
32	BIOINF_KMB_FNS_UNIBA	ss3023745298	Nov 08, 2017 (151)
33	CSHL	ss3343713125	Nov 08, 2017 (151)
34	URBANLAB	ss3646792577	Oct 11, 2018 (152)
35	EGCUT_WGS	ss3655703475	Jul 12, 2019 (153)
36	ACPOP	ss3727491002	Jul 12, 2019 (153)
37	EVA	ss3746816321	Jul 12, 2019 (153)
38	PACBIO	ss3783568288	Jul 12, 2019 (153)
39	PACBIO	ss3789199282	Jul 12, 2019 (153)
40	PACBIO	ss3794071288	Jul 12, 2019 (153)
41	KHV_HUMAN_GENOMES	ss3799816792	Jul 12, 2019 (153)
42	EVA	ss3826427142	Apr 25, 2020 (154)
43	EVA	ss3836608118	Apr 25, 2020 (154)
44	EVA	ss3842017385	Apr 25, 2020 (154)
45	SGDP_PRJ	ss3850020559	Apr 25, 2020 (154)
46	KRGDB	ss3895232794	Apr 25, 2020 (154)
47	TOPMED	ss4468584052	Apr 25, 2021 (155)
48	TOMMO_GENOMICS	ss5146521587	Apr 25, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5244318851	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5444908839	Oct 12, 2022 (156)
51	EVA	ss5506031080	Oct 12, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5517660430	Oct 12, 2022 (156)
53	SANFORD_IMAGENETICS	ss5626605053	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5673730586	Oct 12, 2022 (156)
55	YY_MCH	ss5801265756	Oct 12, 2022 (156)
56	EVA	ss5832674777	Oct 12, 2022 (156)
57	EVA	ss5849110842	Oct 12, 2022 (156)
58	EVA	ss5910273854	Oct 12, 2022 (156)
59	EVA	ss5938399107	Oct 12, 2022 (156)
60	1000Genomes	NC_000001.10 - 155724898	Oct 11, 2018 (152)
61	1000Genomes_30x	NC_000001.11 - 155755107	Oct 12, 2022 (156)
62	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 155724898	Oct 11, 2018 (152)
63	Genetic variation in the Estonian population	NC_000001.10 - 155724898	Oct 11, 2018 (152)
64	The Danish reference pan genome	NC_000001.10 - 155724898	Apr 25, 2020 (154)
65	gnomAD - Genomes	NC_000001.11 - 155755107	Apr 25, 2021 (155)
66	Genome of the Netherlands Release 5	NC_000001.10 - 155724898	Apr 25, 2020 (154)
67	KOREAN population from KRGDB	NC_000001.10 - 155724898	Apr 25, 2020 (154)
68	Northern Sweden	NC_000001.10 - 155724898	Jul 12, 2019 (153)
69	Qatari	NC_000001.10 - 155724898	Apr 25, 2020 (154)
70	SGDP_PRJ	NC_000001.10 - 155724898	Apr 25, 2020 (154)
71	Siberian	NC_000001.10 - 155724898	Apr 25, 2020 (154)
72	8.3KJPN	NC_000001.10 - 155724898	Apr 25, 2021 (155)
73	14KJPN	NC_000001.11 - 155755107	Oct 12, 2022 (156)
74	TopMed	NC_000001.11 - 155755107	Apr 25, 2021 (155)
75	UK 10K study - Twins	NC_000001.10 - 155724898	Oct 11, 2018 (152)
76	ALFA	NC_000001.11 - 155755107	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)
rs59899670	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss80823437	NC_000001.8:152537970:T:C	NC_000001.11:155755106:T:C	(self)
ss164133265, ss165230412, ss199093890, ss205448804, ss276053176, ss290638154, ss1585071186	NC_000001.9:153991521:T:C	NC_000001.11:155755106:T:C	(self)
3747832, 2037558, 1441723, 1710688, 884584, 2410188, 775867, 965013, 2037539, 518244, 4490894, 2037558, ss328954995, ss554706119, ss648418077, ss975689421, ss1292954808, ss1574395333, ss1601228758, ss1644222791, ss1795100627, ss1918923083, ss2019976650, ss2148001890, ss2624496207, ss2697974623, ss2761407948, ss2987764397, ss3343713125, ss3655703475, ss3727491002, ss3746816321, ss3783568288, ss3789199282, ss3794071288, ss3826427142, ss3836608118, ss3850020559, ss3895232794, ss5146521587, ss5506031080, ss5626605053, ss5832674777, ss5938399107	NC_000001.10:155724897:T:C	NC_000001.11:155755106:T:C	(self)
5186365, 27287561, 7567690, 32190387, 2644690324, ss3023745298, ss3646792577, ss3799816792, ss3842017385, ss4468584052, ss5244318851, ss5444908839, ss5517660430, ss5673730586, ss5801265756, ss5849110842, ss5910273854	NC_000001.11:155755106:T:C	NC_000001.11:155755106:T:C	(self)
ss41268299, ss99251605, ss102786208, ss131696243	NT_004487.19:7213539:T:C	NC_000001.11:155755106:T:C	(self)
ss11419527, ss13008659	NT_004668.15:2177298:T:C	NC_000001.11:155755106:T:C	(self)
ss20491881	NT_079484.1:2174729:T:C	NC_000001.11:155755106:T:C	(self)
2410188, ss3895232794	NC_000001.10:155724897:T:G	NC_000001.11:155755106:T:G	(self)
2644690324	NC_000001.11:155755106:T:G	NC_000001.11:155755106:T:G	(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 rs7550402

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

rs7550402