Name: rs7469569
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.

rs7469569

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:137031950 (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>A / T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.331985 (87873/264690, TOPMED)
T=0.332090 (82826/249408, GnomAD_exome)
T=0.341386 (47596/139420, GnomAD) (+ 19 more)
T=0.328286 (39328/119798, ExAC)
T=0.35085 (19696/56138, ALFA)
T=0.25485 (7176/28158, 14KJPN)
T=0.25248 (4225/16734, 8.3KJPN)
T=0.33331 (4329/12988, GO-ESP)
T=0.3065 (1963/6404, 1000G_30x)
T=0.3005 (1505/5008, 1000G)
T=0.3719 (1660/4464, Estonian)
T=0.3521 (1357/3854, ALSPAC)
T=0.3522 (1306/3708, TWINSUK)
T=0.2375 (694/2922, KOREAN)
T=0.2796 (529/1892, HapMap)
T=0.342 (205/600, NorthernSweden)
C=0.125 (67/534, MGP)
T=0.254 (129/508, SGDP_PRJ)
T=0.390 (117/300, FINRISK)
T=0.389 (84/216, Qatari)
T=0.26 (14/54, Siberian)
T=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FUT7 : Intron Variant
LINC02908 : 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	56138	T=0.35085	C=0.64915
European	Sub	37942	T=0.36052	C=0.63948
African	Sub	5934	T=0.3043	C=0.6957
African Others	Sub	184	T=0.348	C=0.652
African American	Sub	5750	T=0.3030	C=0.6970
Asian	Sub	498	T=0.285	C=0.715
East Asian	Sub	400	T=0.278	C=0.723
Other Asian	Sub	98	T=0.32	C=0.68
Latin American 1	Sub	356	T=0.368	C=0.632
Latin American 2	Sub	5466	T=0.3421	C=0.6579
South Asian	Sub	154	T=0.357	C=0.643
Other	Sub	5788	T=0.3478	C=0.6522

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=0.331985	C=0.668015
gnomAD - Exomes	Global	Study-wide	249408	T=0.332090	C=0.667910
gnomAD - Exomes	European	Sub	133818	T=0.354661	C=0.645339
gnomAD - Exomes	Asian	Sub	48964	T=0.26560	C=0.73440
gnomAD - Exomes	American	Sub	34514	T=0.33908	C=0.66092
gnomAD - Exomes	African	Sub	16042	T=0.29491	C=0.70509
gnomAD - Exomes	Ashkenazi Jewish	Sub	9974	T=0.3847	C=0.6153
gnomAD - Exomes	Other	Sub	6096	T=0.3428	C=0.6572
gnomAD - Genomes	Global	Study-wide	139420	T=0.341386	C=0.658614
gnomAD - Genomes	European	Sub	75582	T=0.36060	C=0.63940
gnomAD - Genomes	African	Sub	41672	T=0.30781	C=0.69219
gnomAD - Genomes	American	Sub	13602	T=0.34429	C=0.65571
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	T=0.3894	C=0.6106
gnomAD - Genomes	East Asian	Sub	3106	T=0.2624	C=0.7376
gnomAD - Genomes	Other	Sub	2140	T=0.3383	C=0.6617
ExAC	Global	Study-wide	119798	T=0.328286	C=0.671714
ExAC	Europe	Sub	72042	T=0.35365	C=0.64635
ExAC	Asian	Sub	25120	T=0.26250	C=0.73750
ExAC	American	Sub	11506	T=0.33704	C=0.66296
ExAC	African	Sub	10242	T=0.30121	C=0.69879
ExAC	Other	Sub	888	T=0.330	C=0.670
Allele Frequency Aggregator	Total	Global	56138	T=0.35085	C=0.64915
Allele Frequency Aggregator	European	Sub	37942	T=0.36052	C=0.63948
Allele Frequency Aggregator	African	Sub	5934	T=0.3043	C=0.6957
Allele Frequency Aggregator	Other	Sub	5788	T=0.3478	C=0.6522
Allele Frequency Aggregator	Latin American 2	Sub	5466	T=0.3421	C=0.6579
Allele Frequency Aggregator	Asian	Sub	498	T=0.285	C=0.715
Allele Frequency Aggregator	Latin American 1	Sub	356	T=0.368	C=0.632
Allele Frequency Aggregator	South Asian	Sub	154	T=0.357	C=0.643
14KJPN	JAPANESE	Study-wide	28158	T=0.25485	C=0.74515
8.3KJPN	JAPANESE	Study-wide	16734	T=0.25248	C=0.74752
GO Exome Sequencing Project	Global	Study-wide	12988	T=0.33331	C=0.66669
GO Exome Sequencing Project	European American	Sub	8588	T=0.3505	C=0.6495
GO Exome Sequencing Project	African American	Sub	4400	T=0.2998	C=0.7002
1000Genomes_30x	Global	Study-wide	6404	T=0.3065	C=0.6935
1000Genomes_30x	African	Sub	1786	T=0.2872	C=0.7128
1000Genomes_30x	Europe	Sub	1266	T=0.3791	C=0.6209
1000Genomes_30x	South Asian	Sub	1202	T=0.2521	C=0.7479
1000Genomes_30x	East Asian	Sub	1170	T=0.2350	C=0.7650
1000Genomes_30x	American	Sub	980	T=0.400	C=0.600
1000Genomes	Global	Study-wide	5008	T=0.3005	C=0.6995
1000Genomes	African	Sub	1322	T=0.2852	C=0.7148
1000Genomes	East Asian	Sub	1008	T=0.2321	C=0.7679
1000Genomes	Europe	Sub	1006	T=0.3708	C=0.6292
1000Genomes	South Asian	Sub	978	T=0.252	C=0.748
1000Genomes	American	Sub	694	T=0.396	C=0.604
Genetic variation in the Estonian population	Estonian	Study-wide	4464	T=0.3719	C=0.6281
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.3521	C=0.6479
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.3522	C=0.6478
KOREAN population from KRGDB	KOREAN	Study-wide	2922	T=0.2375	A=0.0000, C=0.7625
HapMap	Global	Study-wide	1892	T=0.2796	C=0.7204
HapMap	American	Sub	770	T=0.295	C=0.705
HapMap	African	Sub	692	T=0.275	C=0.725
HapMap	Asian	Sub	254	T=0.220	C=0.780
HapMap	Europe	Sub	176	T=0.318	C=0.682
Northern Sweden	ACPOP	Study-wide	600	T=0.342	C=0.658
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.875	C=0.125
SGDP_PRJ	Global	Study-wide	508	T=0.254	C=0.746
FINRISK	Finnish from FINRISK project	Study-wide	300	T=0.390	C=0.610
Qatari	Global	Study-wide	216	T=0.389	C=0.611
Siberian	Global	Study-wide	54	T=0.26	C=0.74
The Danish reference pan genome	Danish	Study-wide	40	T=0.38	C=0.62

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 9	NC_000009.12:g.137031950T>A
GRCh38.p14 chr 9	NC_000009.12:g.137031950T>C
GRCh37.p13 chr 9	NC_000009.11:g.139926402T>A
GRCh37.p13 chr 9	NC_000009.11:g.139926402T>C
ABCA2 RefSeqGene	NG_011789.1:g.1973A>T
ABCA2 RefSeqGene	NG_011789.1:g.1973A>G
FUT7 RefSeqGene	NG_007527.1:g.5891A>T
FUT7 RefSeqGene	NG_007527.1:g.5891A>G

Gene: FUT7, fucosyltransferase 7 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FUT7 transcript	NM_004479.4:c.13+29A>T	N/A	Intron Variant

Gene: LINC02908, long intergenic non-protein coding RNA 2908 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02908 transcript	NR_171031.1:n.	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.

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=	A	C
GRCh38.p14 chr 9	NC_000009.12:g.137031950=	NC_000009.12:g.137031950T>A	NC_000009.12:g.137031950T>C
GRCh37.p13 chr 9	NC_000009.11:g.139926402=	NC_000009.11:g.139926402T>A	NC_000009.11:g.139926402T>C
ABCA2 RefSeqGene	NG_011789.1:g.1973=	NG_011789.1:g.1973A>T	NG_011789.1:g.1973A>G
FUT7 RefSeqGene	NG_007527.1:g.5891=	NG_007527.1:g.5891A>T	NG_007527.1:g.5891A>G
FUT7 transcript	NM_004479.3:c.13+29=	NM_004479.3:c.13+29A>T	NM_004479.3:c.13+29A>G
FUT7 transcript	NM_004479.4:c.13+29=	NM_004479.4:c.13+29A>T	NM_004479.4:c.13+29A>G
C9orf139 transcript	NM_207511.1:c.-1066-48=	NM_207511.1:c.-1066-48T>A	NM_207511.1:c.-1066-48T>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, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss11279706	Jul 11, 2003 (116)
2	WI_SSAHASNP	ss14360162	Dec 05, 2003 (119)
3	SC_SNP	ss15717425	Feb 27, 2004 (120)
4	CSHL-HAPMAP	ss17259672	Feb 27, 2004 (120)
5	SSAHASNP	ss22828301	Apr 05, 2004 (121)
6	ILLUMINA	ss74967027	Dec 06, 2007 (129)
7	BCMHGSC_JDW	ss94201479	Mar 25, 2008 (129)
8	HUMANGENOME_JCVI	ss97837809	Feb 04, 2009 (130)
9	BGI	ss105708768	Feb 04, 2009 (130)
10	1000GENOMES	ss109141697	Jan 23, 2009 (130)
11	ILLUMINA-UK	ss115817480	Feb 14, 2009 (130)
12	KRIBB_YJKIM	ss119554659	Dec 01, 2009 (131)
13	ENSEMBL	ss133566070	Dec 01, 2009 (131)
14	ENSEMBL	ss144409585	Dec 01, 2009 (131)
15	ILLUMINA	ss152536285	Dec 01, 2009 (131)
16	GMI	ss158068454	Dec 01, 2009 (131)
17	ILLUMINA	ss159102614	Dec 01, 2009 (131)
18	ILLUMINA	ss159845994	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss165076400	Jul 04, 2010 (132)
20	ILLUMINA	ss168870635	Jul 04, 2010 (132)
21	ILLUMINA	ss174379213	Jul 04, 2010 (132)
22	BUSHMAN	ss201013036	Jul 04, 2010 (132)
23	1000GENOMES	ss210874831	Jul 14, 2010 (132)
24	1000GENOMES	ss224508560	Jul 14, 2010 (132)
25	1000GENOMES	ss235009601	Jul 15, 2010 (132)
26	1000GENOMES	ss241751218	Jul 15, 2010 (132)
27	GMI	ss280436979	May 04, 2012 (137)
28	GMI	ss286109528	Apr 25, 2013 (138)
29	PJP	ss294392025	May 09, 2011 (134)
30	ILLUMINA	ss479154411	Sep 08, 2015 (146)
31	1000GENOMES	ss490990386	May 04, 2012 (137)
32	CLINSEQ_SNP	ss491947155	May 04, 2012 (137)
33	ILLUMINA	ss536521767	Sep 08, 2015 (146)
34	SSMP	ss656200488	Apr 25, 2013 (138)
35	NHLBI-ESP	ss712929480	Apr 25, 2013 (138)
36	ILLUMINA	ss832615410	Jul 13, 2019 (153)
37	JMKIDD_LAB	ss974473411	Aug 21, 2014 (142)
38	EVA-GONL	ss987087440	Aug 21, 2014 (142)
39	JMKIDD_LAB	ss1067509813	Aug 21, 2014 (142)
40	JMKIDD_LAB	ss1076682624	Aug 21, 2014 (142)
41	1000GENOMES	ss1335872389	Aug 21, 2014 (142)
42	DDI	ss1431991001	Apr 01, 2015 (144)
43	EVA_GENOME_DK	ss1583298371	Apr 01, 2015 (144)
44	EVA_FINRISK	ss1584066125	Apr 01, 2015 (144)
45	EVA_DECODE	ss1596735231	Apr 01, 2015 (144)
46	EVA_UK10K_ALSPAC	ss1623780241	Apr 01, 2015 (144)
47	EVA_UK10K_TWINSUK	ss1666774274	Apr 01, 2015 (144)
48	EVA_EXAC	ss1689767648	Apr 01, 2015 (144)
49	EVA_MGP	ss1711244076	Apr 01, 2015 (144)
50	EVA_SVP	ss1713148569	Apr 01, 2015 (144)
51	WEILL_CORNELL_DGM	ss1930404196	Feb 12, 2016 (147)
52	JJLAB	ss2025925110	Sep 14, 2016 (149)
53	USC_VALOUEV	ss2154163540	Dec 20, 2016 (150)
54	HUMAN_LONGEVITY	ss2315296230	Dec 20, 2016 (150)
55	SYSTEMSBIOZJU	ss2627430662	Nov 08, 2017 (151)
56	GRF	ss2710049006	Nov 08, 2017 (151)
57	GNOMAD	ss2738038554	Nov 08, 2017 (151)
58	GNOMAD	ss2748322038	Nov 08, 2017 (151)
59	GNOMAD	ss2884388521	Nov 08, 2017 (151)
60	SWEGEN	ss3005763715	Nov 08, 2017 (151)
61	ILLUMINA	ss3022979336	Nov 08, 2017 (151)
62	BIOINF_KMB_FNS_UNIBA	ss3026745166	Nov 08, 2017 (151)
63	CSHL	ss3348906236	Nov 08, 2017 (151)
64	ILLUMINA	ss3630383018	Oct 12, 2018 (152)
65	ILLUMINA	ss3636987756	Oct 12, 2018 (152)
66	ILLUMINA	ss3638842986	Oct 12, 2018 (152)
67	ILLUMINA	ss3638842987	Oct 12, 2018 (152)
68	ILLUMINA	ss3643767296	Oct 12, 2018 (152)
69	OMUKHERJEE_ADBS	ss3646400826	Oct 12, 2018 (152)
70	URBANLAB	ss3649262444	Oct 12, 2018 (152)
71	ILLUMINA	ss3653536551	Oct 12, 2018 (152)
72	EGCUT_WGS	ss3673300549	Jul 13, 2019 (153)
73	EVA_DECODE	ss3724969333	Jul 13, 2019 (153)
74	ILLUMINA	ss3726654795	Jul 13, 2019 (153)
75	ACPOP	ss3736966416	Jul 13, 2019 (153)
76	EVA	ss3769822420	Jul 13, 2019 (153)
77	KHV_HUMAN_GENOMES	ss3812981905	Jul 13, 2019 (153)
78	EVA	ss3824490212	Apr 26, 2020 (154)
79	EVA	ss3825768709	Apr 26, 2020 (154)
80	EVA	ss3831912832	Apr 26, 2020 (154)
81	EVA	ss3839485289	Apr 26, 2020 (154)
82	EVA	ss3844951152	Apr 26, 2020 (154)
83	SGDP_PRJ	ss3873299435	Apr 26, 2020 (154)
84	KRGDB	ss3921215319	Apr 26, 2020 (154)
85	FSA-LAB	ss3984436462	Apr 26, 2021 (155)
86	FSA-LAB	ss3984436463	Apr 26, 2021 (155)
87	EVA	ss3986471457	Apr 26, 2021 (155)
88	TOPMED	ss4839185541	Apr 26, 2021 (155)
89	TOMMO_GENOMICS	ss5195791488	Apr 26, 2021 (155)
90	1000G_HIGH_COVERAGE	ss5282556997	Oct 16, 2022 (156)
91	TRAN_CS_UWATERLOO	ss5314427465	Oct 16, 2022 (156)
92	EVA	ss5390940999	Oct 16, 2022 (156)
93	HUGCELL_USP	ss5478380356	Oct 16, 2022 (156)
94	1000G_HIGH_COVERAGE	ss5575785891	Oct 16, 2022 (156)
95	EVA	ss5624190113	Oct 16, 2022 (156)
96	SANFORD_IMAGENETICS	ss5648469308	Oct 16, 2022 (156)
97	TOMMO_GENOMICS	ss5740494374	Oct 16, 2022 (156)
98	EVA	ss5800061235	Oct 16, 2022 (156)
99	EVA	ss5800156427	Oct 16, 2022 (156)
100	YY_MCH	ss5811098958	Oct 16, 2022 (156)
101	EVA	ss5829896357	Oct 16, 2022 (156)
102	EVA	ss5848736821	Oct 16, 2022 (156)
103	EVA	ss5856978778	Oct 16, 2022 (156)
104	EVA	ss5918452695	Oct 16, 2022 (156)
105	EVA	ss5936543442	Oct 16, 2022 (156)
106	EVA	ss5977683690	Oct 16, 2022 (156)
107	EVA	ss5980587123	Oct 16, 2022 (156)
108	1000Genomes	NC_000009.11 - 139926402	Oct 12, 2018 (152)
109	1000Genomes_30x	NC_000009.12 - 137031950	Oct 16, 2022 (156)
110	The Avon Longitudinal Study of Parents and Children	NC_000009.11 - 139926402	Oct 12, 2018 (152)
111	Genetic variation in the Estonian population	NC_000009.11 - 139926402	Oct 12, 2018 (152)
112	ExAC	NC_000009.11 - 139926402	Oct 12, 2018 (152)
113	FINRISK	NC_000009.11 - 139926402	Apr 26, 2020 (154)
114	The Danish reference pan genome	NC_000009.11 - 139926402	Apr 26, 2020 (154)
115	gnomAD - Genomes	NC_000009.12 - 137031950	Apr 26, 2021 (155)
116	gnomAD - Exomes	NC_000009.11 - 139926402	Jul 13, 2019 (153)
117	GO Exome Sequencing Project	NC_000009.11 - 139926402	Oct 12, 2018 (152)
118	HapMap	NC_000009.12 - 137031950	Apr 26, 2020 (154)
119	KOREAN population from KRGDB	NC_000009.11 - 139926402	Apr 26, 2020 (154)
120	Medical Genome Project healthy controls from Spanish population	NC_000009.11 - 139926402	Apr 26, 2020 (154)
121	Northern Sweden	NC_000009.11 - 139926402	Jul 13, 2019 (153)
122	Qatari	NC_000009.11 - 139926402	Apr 26, 2020 (154)
123	SGDP_PRJ	NC_000009.11 - 139926402	Apr 26, 2020 (154)
124	Siberian	NC_000009.11 - 139926402	Apr 26, 2020 (154)
125	8.3KJPN	NC_000009.11 - 139926402	Apr 26, 2021 (155)
126	14KJPN	NC_000009.12 - 137031950	Oct 16, 2022 (156)
127	TopMed	NC_000009.12 - 137031950	Apr 26, 2021 (155)
128	UK 10K study - Twins	NC_000009.11 - 139926402	Oct 12, 2018 (152)
129	ALFA	NC_000009.12 - 137031950	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
28392713, ss3921215319	NC_000009.11:139926401:T:A	NC_000009.12:137031949:T:A	(self)
ss94201479, ss109141697, ss115817480, ss165076400, ss201013036, ss210874831, ss280436979, ss286109528, ss294392025, ss491947155, ss1596735231, ss1713148569, ss3643767296	NC_000009.10:139046222:T:C	NC_000009.12:137031949:T:C	(self)
48204859, 26787470, 19038797, 9911309, 62586, 9463308, 7230214, 947946, 28392713, 359836, 10251281, 12446126, 25316415, 6679894, 53760795, 26787470, ss224508560, ss235009601, ss241751218, ss479154411, ss490990386, ss536521767, ss656200488, ss712929480, ss832615410, ss974473411, ss987087440, ss1067509813, ss1076682624, ss1335872389, ss1431991001, ss1583298371, ss1584066125, ss1623780241, ss1666774274, ss1689767648, ss1711244076, ss1930404196, ss2025925110, ss2154163540, ss2627430662, ss2710049006, ss2738038554, ss2748322038, ss2884388521, ss3005763715, ss3022979336, ss3348906236, ss3630383018, ss3636987756, ss3638842986, ss3638842987, ss3646400826, ss3653536551, ss3673300549, ss3736966416, ss3769822420, ss3824490212, ss3825768709, ss3831912832, ss3839485289, ss3873299435, ss3921215319, ss3984436462, ss3984436463, ss3986471457, ss5195791488, ss5390940999, ss5624190113, ss5648469308, ss5800061235, ss5800156427, ss5829896357, ss5848736821, ss5936543442, ss5977683690, ss5980587123	NC_000009.11:139926401:T:C	NC_000009.12:137031949:T:C	(self)
63311826, 340629476, 3937887, 74331478, 676563102, 4103592971, ss2315296230, ss3026745166, ss3649262444, ss3724969333, ss3726654795, ss3812981905, ss3844951152, ss4839185541, ss5282556997, ss5314427465, ss5478380356, ss5575785891, ss5740494374, ss5811098958, ss5856978778, ss5918452695	NC_000009.12:137031949:T:C	NC_000009.12:137031949:T:C	(self)
ss11279706, ss14360162, ss15717425, ss17259672, ss22828301	NT_024000.15:677480:T:C	NC_000009.12:137031949:T:C	(self)
ss74967027, ss97837809, ss105708768, ss119554659, ss133566070, ss144409585, ss152536285, ss158068454, ss159102614, ss159845994, ss168870635, ss174379213	NT_024000.16:709404:T:C	NC_000009.12:137031949: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 rs7469569

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
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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.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs7469569