Name: rs11568544
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.

rs11568544

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:100401921 (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>C / A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.273569 (72411/264690, TOPMED)
G=0.28034 (9859/35168, ALFA)
G=0.05882 (1662/28258, 14KJPN) (+ 20 more)
G=0.06032 (1011/16760, 8.3KJPN)
G=0.2082 (1333/6404, 1000G_30x)
G=0.2097 (1050/5008, 1000G)
G=0.3099 (1415/4566, GO-ESP)
G=0.3786 (1696/4480, Estonian)
G=0.3770 (1453/3854, ALSPAC)
G=0.3765 (1396/3708, TWINSUK)
G=0.0705 (206/2922, KOREAN)
G=0.1804 (341/1890, HapMap)
G=0.0710 (130/1832, Korea1K)
G=0.359 (358/998, GoNL)
G=0.222 (139/626, Chileans)
G=0.378 (227/600, NorthernSweden)
G=0.220 (121/550, PharmGKB)
G=0.425 (227/534, MGP)
G=0.394 (85/216, Qatari)
G=0.033 (7/210, Vietnamese)
A=0.422 (70/166, SGDP_PRJ)
G=0.23 (9/40, GENOME_DK)
A=0.41 (14/34, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: SLC17A8 : Intron Variant
LOC124903108 : 2KB Upstream 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	35168	A=0.71966	C=0.00000, G=0.28034
European	Sub	25460	A=0.67321	C=0.00000, G=0.32679
African	Sub	4152	A=0.9114	C=0.0000, G=0.0886
African Others	Sub	142	A=0.894	C=0.000, G=0.106
African American	Sub	4010	A=0.9120	C=0.0000, G=0.0880
Asian	Sub	182	A=0.984	C=0.000, G=0.016
East Asian	Sub	126	A=0.984	C=0.000, G=0.016
Other Asian	Sub	56	A=0.98	C=0.00, G=0.02
Latin American 1	Sub	244	A=0.791	C=0.000, G=0.209
Latin American 2	Sub	2646	A=0.8356	C=0.0000, G=0.1644
South Asian	Sub	96	A=0.86	C=0.00, G=0.14
Other	Sub	2388	A=0.7198	C=0.0000, G=0.2802

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=0.726431	G=0.273569
Allele Frequency Aggregator	Total	Global	35168	A=0.71966	C=0.00000, G=0.28034
Allele Frequency Aggregator	European	Sub	25460	A=0.67321	C=0.00000, G=0.32679
Allele Frequency Aggregator	African	Sub	4152	A=0.9114	C=0.0000, G=0.0886
Allele Frequency Aggregator	Latin American 2	Sub	2646	A=0.8356	C=0.0000, G=0.1644
Allele Frequency Aggregator	Other	Sub	2388	A=0.7198	C=0.0000, G=0.2802
Allele Frequency Aggregator	Latin American 1	Sub	244	A=0.791	C=0.000, G=0.209
Allele Frequency Aggregator	Asian	Sub	182	A=0.984	C=0.000, G=0.016
Allele Frequency Aggregator	South Asian	Sub	96	A=0.86	C=0.00, G=0.14
14KJPN	JAPANESE	Study-wide	28258	A=0.94118	G=0.05882
8.3KJPN	JAPANESE	Study-wide	16760	A=0.93968	G=0.06032
1000Genomes_30x	Global	Study-wide	6404	A=0.7918	G=0.2082
1000Genomes_30x	African	Sub	1786	A=0.8544	G=0.1456
1000Genomes_30x	Europe	Sub	1266	A=0.5806	G=0.4194
1000Genomes_30x	South Asian	Sub	1202	A=0.7829	G=0.2171
1000Genomes_30x	East Asian	Sub	1170	A=0.9598	G=0.0402
1000Genomes_30x	American	Sub	980	A=0.761	G=0.239
1000Genomes	Global	Study-wide	5008	A=0.7903	G=0.2097
1000Genomes	African	Sub	1322	A=0.8585	G=0.1415
1000Genomes	East Asian	Sub	1008	A=0.9583	G=0.0417
1000Genomes	Europe	Sub	1006	A=0.5755	G=0.4245
1000Genomes	South Asian	Sub	978	A=0.774	G=0.226
1000Genomes	American	Sub	694	A=0.751	G=0.249
GO Exome Sequencing Project	Global	Study-wide	4566	A=0.6901	G=0.3099
GO Exome Sequencing Project	European American	Sub	3182	A=0.6314	G=0.3686
GO Exome Sequencing Project	African American	Sub	1384	A=0.8251	G=0.1749
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.6214	G=0.3786
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.6230	G=0.3770
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.6235	G=0.3765
KOREAN population from KRGDB	KOREAN	Study-wide	2922	A=0.9295	G=0.0705
HapMap	Global	Study-wide	1890	A=0.8196	G=0.1804
HapMap	American	Sub	768	A=0.789	G=0.211
HapMap	African	Sub	692	A=0.861	G=0.139
HapMap	Asian	Sub	254	A=0.953	G=0.047
HapMap	Europe	Sub	176	A=0.597	G=0.403
Korean Genome Project	KOREAN	Study-wide	1832	A=0.9290	G=0.0710
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.641	G=0.359
Chileans	Chilean	Study-wide	626	A=0.778	G=0.222
Northern Sweden	ACPOP	Study-wide	600	A=0.622	G=0.378
PharmGKB Aggregated	Global	Study-wide	550	A=0.780	G=0.220
PharmGKB Aggregated	PA129623036	Sub	550	A=0.780	G=0.220
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	A=0.575	G=0.425
Qatari	Global	Study-wide	216	A=0.606	G=0.394
A Vietnamese Genetic Variation Database	Global	Study-wide	210	A=0.967	G=0.033
SGDP_PRJ	Global	Study-wide	166	A=0.422	G=0.578
The Danish reference pan genome	Danish	Study-wide	40	A=0.78	G=0.23
Siberian	Global	Study-wide	34	A=0.41	G=0.59

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 12	NC_000012.12:g.100401921A>C
GRCh38.p14 chr 12	NC_000012.12:g.100401921A>G
GRCh37.p13 chr 12	NC_000012.11:g.100795699A>C
GRCh37.p13 chr 12	NC_000012.11:g.100795699A>G
SLC17A8 RefSeqGene	NG_021175.1:g.49843A>C
SLC17A8 RefSeqGene	NG_021175.1:g.49843A>G

Gene: SLC17A8, solute carrier family 17 member 8 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC17A8 transcript variant 2	NM_001145288.2:c.763+58A>C	N/A	Intron Variant
SLC17A8 transcript variant 1	NM_139319.3:c.763+58A>C	N/A	Intron Variant

Gene: LOC124903108, uncharacterized LOC124903108 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124903108 transcript	XR_007063645.1:n.	N/A	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.

Allele: G (allele ID: 1237687 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001649693.2	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	A=	C	G
GRCh38.p14 chr 12	NC_000012.12:g.100401921=	NC_000012.12:g.100401921A>C	NC_000012.12:g.100401921A>G
GRCh37.p13 chr 12	NC_000012.11:g.100795699=	NC_000012.11:g.100795699A>C	NC_000012.11:g.100795699A>G
SLC17A8 RefSeqGene	NG_021175.1:g.49843=	NG_021175.1:g.49843A>C	NG_021175.1:g.49843A>G
SLC17A8 transcript variant 2	NM_001145288.1:c.763+58=	NM_001145288.1:c.763+58A>C	NM_001145288.1:c.763+58A>G
SLC17A8 transcript variant 2	NM_001145288.2:c.763+58=	NM_001145288.2:c.763+58A>C	NM_001145288.2:c.763+58A>G
SLC17A8 transcript variant 1	NM_139319.2:c.763+58=	NM_139319.2:c.763+58A>C	NM_139319.2:c.763+58A>G
SLC17A8 transcript variant 1	NM_139319.3:c.763+58=	NM_139319.3:c.763+58A>C	NM_139319.3:c.763+58A>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#.

91 SubSNP, 25 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	ILLUMINA	ss65774997	Oct 15, 2006 (127)
2	PHARMGKB_PMT	ss69371683	May 17, 2007 (127)
3	ILLUMINA	ss74879812	Dec 06, 2007 (129)
4	AFFY	ss76794487	Dec 08, 2007 (129)
5	HUMANGENOME_JCVI	ss97335169	Feb 05, 2009 (130)
6	1000GENOMES	ss112390137	Jan 25, 2009 (130)
7	KRIBB_YJKIM	ss119689242	Dec 01, 2009 (131)
8	ENSEMBL	ss143345095	Dec 01, 2009 (131)
9	ILLUMINA	ss171292312	Jul 04, 2010 (132)
10	COMPLETE_GENOMICS	ss175251225	Jul 04, 2010 (132)
11	BUSHMAN	ss198605384	Jul 04, 2010 (132)
12	1000GENOMES	ss211329097	Jul 14, 2010 (132)
13	1000GENOMES	ss225924063	Jul 14, 2010 (132)
14	1000GENOMES	ss236061718	Jul 15, 2010 (132)
15	BL	ss255320279	May 09, 2011 (134)
16	GMI	ss286616208	Apr 25, 2013 (138)
17	GMI	ss475787094	May 04, 2012 (137)
18	ILLUMINA	ss483138158	May 04, 2012 (137)
19	ILLUMINA	ss483387247	May 04, 2012 (137)
20	ILLUMINA	ss535599756	Sep 08, 2015 (146)
21	TISHKOFF	ss563360669	Apr 25, 2013 (138)
22	SSMP	ss658941853	Apr 25, 2013 (138)
23	NHLBI-ESP	ss713112600	Apr 25, 2013 (138)
24	ILLUMINA	ss780258210	Aug 21, 2014 (142)
25	ILLUMINA	ss782136798	Aug 21, 2014 (142)
26	ILLUMINA	ss835744010	Aug 21, 2014 (142)
27	EVA-GONL	ss989883804	Aug 21, 2014 (142)
28	PMT	ss1040218650	Aug 21, 2014 (142)
29	JMKIDD_LAB	ss1078716861	Aug 21, 2014 (142)
30	1000GENOMES	ss1346351136	Aug 21, 2014 (142)
31	DDI	ss1427033337	Apr 01, 2015 (144)
32	EVA_GENOME_DK	ss1576479966	Apr 01, 2015 (144)
33	EVA_UK10K_ALSPAC	ss1629288507	Apr 01, 2015 (144)
34	EVA_DECODE	ss1641985631	Apr 01, 2015 (144)
35	EVA_UK10K_TWINSUK	ss1672282540	Apr 01, 2015 (144)
36	EVA_MGP	ss1711339914	Apr 01, 2015 (144)
37	EVA_SVP	ss1713352048	Apr 01, 2015 (144)
38	HAMMER_LAB	ss1807387964	Sep 08, 2015 (146)
39	WEILL_CORNELL_DGM	ss1933238680	Feb 12, 2016 (147)
40	JJLAB	ss2027374841	Sep 14, 2016 (149)
41	USC_VALOUEV	ss2155721057	Dec 20, 2016 (150)
42	HUMAN_LONGEVITY	ss2192584821	Dec 20, 2016 (150)
43	ILLUMINA	ss2632999133	Nov 08, 2017 (151)
44	GRF	ss2700077641	Nov 08, 2017 (151)
45	GNOMAD	ss2914362572	Nov 08, 2017 (151)
46	SWEGEN	ss3010231276	Nov 08, 2017 (151)
47	BIOINF_KMB_FNS_UNIBA	ss3027497973	Nov 08, 2017 (151)
48	CSHL	ss3350216912	Nov 08, 2017 (151)
49	ILLUMINA	ss3626950736	Oct 12, 2018 (152)
50	ILLUMINA	ss3631006085	Oct 12, 2018 (152)
51	ILLUMINA	ss3637981918	Oct 12, 2018 (152)
52	ILLUMINA	ss3641807530	Oct 12, 2018 (152)
53	ILLUMINA	ss3642973933	Oct 12, 2018 (152)
54	OMUKHERJEE_ADBS	ss3646445991	Oct 12, 2018 (152)
55	URBANLAB	ss3649909529	Oct 12, 2018 (152)
56	EGCUT_WGS	ss3677525440	Jul 13, 2019 (153)
57	EVA_DECODE	ss3694321606	Jul 13, 2019 (153)
58	ACPOP	ss3739318515	Jul 13, 2019 (153)
59	EVA	ss3750878246	Jul 13, 2019 (153)
60	PACBIO	ss3787316706	Jul 13, 2019 (153)
61	PACBIO	ss3792402943	Jul 13, 2019 (153)
62	PACBIO	ss3797285987	Jul 13, 2019 (153)
63	KHV_HUMAN_GENOMES	ss3816211829	Jul 13, 2019 (153)
64	EVA	ss3824760957	Apr 27, 2020 (154)
65	EVA	ss3833290816	Apr 27, 2020 (154)
66	EVA	ss3840218211	Apr 27, 2020 (154)
67	EVA	ss3845706407	Apr 27, 2020 (154)
68	SGDP_PRJ	ss3878964283	Apr 27, 2020 (154)
69	KRGDB	ss3927685780	Apr 27, 2020 (154)
70	KOGIC	ss3972578755	Apr 27, 2020 (154)
71	FSA-LAB	ss3984035086	Apr 25, 2021 (155)
72	EVA	ss3986581990	Apr 25, 2021 (155)
73	TOPMED	ss4930260455	Apr 25, 2021 (155)
74	TOMMO_GENOMICS	ss5207839238	Apr 25, 2021 (155)
75	1000G_HIGH_COVERAGE	ss5291982305	Oct 16, 2022 (156)
76	EVA	ss5315643722	Oct 16, 2022 (156)
77	EVA	ss5407766938	Oct 16, 2022 (156)
78	HUGCELL_USP	ss5486609012	Oct 16, 2022 (156)
79	1000G_HIGH_COVERAGE	ss5590086915	Oct 16, 2022 (156)
80	EVA	ss5623958796	Oct 16, 2022 (156)
81	EVA	ss5624035643	Oct 16, 2022 (156)
82	SANFORD_IMAGENETICS	ss5653818158	Oct 16, 2022 (156)
83	TOMMO_GENOMICS	ss5758065860	Oct 16, 2022 (156)
84	EVA	ss5800065485	Oct 16, 2022 (156)
85	YY_MCH	ss5813584243	Oct 16, 2022 (156)
86	EVA	ss5838415550	Oct 16, 2022 (156)
87	EVA	ss5848360209	Oct 16, 2022 (156)
88	EVA	ss5905729269	Oct 16, 2022 (156)
89	EVA	ss5936554221	Oct 16, 2022 (156)
90	EVA	ss5945212394	Oct 16, 2022 (156)
91	EVA	ss5981277815	Oct 16, 2022 (156)
92	1000Genomes	NC_000012.11 - 100795699	Oct 12, 2018 (152)
93	1000Genomes_30x	NC_000012.12 - 100401921	Oct 16, 2022 (156)
94	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 100795699	Oct 12, 2018 (152)
95	Chileans	NC_000012.11 - 100795699	Apr 27, 2020 (154)
96	Genetic variation in the Estonian population	NC_000012.11 - 100795699	Oct 12, 2018 (152)
97	The Danish reference pan genome	NC_000012.11 - 100795699	Apr 27, 2020 (154)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 417245496 (NC_000012.12:100401920:A:C 3/140048) Row 417245497 (NC_000012.12:100401920:A:G 41445/139990)	-	Apr 25, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 417245496 (NC_000012.12:100401920:A:C 3/140048) Row 417245497 (NC_000012.12:100401920:A:G 41445/139990)	-	Apr 25, 2021 (155)
100	GO Exome Sequencing Project	NC_000012.11 - 100795699	Oct 12, 2018 (152)
101	Genome of the Netherlands Release 5	NC_000012.11 - 100795699	Apr 27, 2020 (154)
102	HapMap	NC_000012.12 - 100401921	Apr 27, 2020 (154)
103	KOREAN population from KRGDB	NC_000012.11 - 100795699	Apr 27, 2020 (154)
104	Korean Genome Project	NC_000012.12 - 100401921	Apr 27, 2020 (154)
105	Medical Genome Project healthy controls from Spanish population	NC_000012.11 - 100795699	Apr 27, 2020 (154)
106	Northern Sweden	NC_000012.11 - 100795699	Jul 13, 2019 (153)
107	PharmGKB Aggregated	NC_000012.12 - 100401921	Apr 27, 2020 (154)
108	Qatari	NC_000012.11 - 100795699	Apr 27, 2020 (154)
109	SGDP_PRJ	NC_000012.11 - 100795699	Apr 27, 2020 (154)
110	Siberian	NC_000012.11 - 100795699	Apr 27, 2020 (154)
111	8.3KJPN	NC_000012.11 - 100795699	Apr 25, 2021 (155)
112	14KJPN	NC_000012.12 - 100401921	Oct 16, 2022 (156)
113	TopMed	NC_000012.12 - 100401921	Apr 25, 2021 (155)
114	UK 10K study - Twins	NC_000012.11 - 100795699	Oct 12, 2018 (152)
115	A Vietnamese Genetic Variation Database	NC_000012.11 - 100795699	Jul 13, 2019 (153)
116	ALFA	NC_000012.12 - 100401921	Apr 25, 2021 (155)
117	ClinVar	RCV001649693.2	Oct 16, 2022 (156)

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)
rs45506994	Mar 05, 2008 (129)
rs56615016	Mar 05, 2008 (129)
rs117443983	Aug 16, 2010 (132)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss2914362572	NC_000012.11:100795698:A:C	NC_000012.12:100401920:A:C	(self)
8621149248	NC_000012.12:100401920:A:C	NC_000012.12:100401920:A:C	(self)
ss112390137, ss175251225, ss198605384, ss211329097, ss255320279, ss286616208, ss475787094, ss483138158, ss1641985631, ss1713352048, ss3642973933	NC_000012.10:99319829:A:G	NC_000012.12:100401920:A:G	(self)
59151255, 32843693, 107518, 23263688, 3098292, 1218405, 14654159, 34863174, 455674, 12603380, 15280610, 30981263, 8237411, 65808545, 32843693, 7290818, ss225924063, ss236061718, ss483387247, ss535599756, ss563360669, ss658941853, ss713112600, ss780258210, ss782136798, ss835744010, ss989883804, ss1040218650, ss1078716861, ss1346351136, ss1427033337, ss1576479966, ss1629288507, ss1672282540, ss1711339914, ss1807387964, ss1933238680, ss2027374841, ss2155721057, ss2632999133, ss2700077641, ss2914362572, ss3010231276, ss3350216912, ss3626950736, ss3631006085, ss3637981918, ss3641807530, ss3646445991, ss3677525440, ss3739318515, ss3750878246, ss3787316706, ss3792402943, ss3797285987, ss3824760957, ss3833290816, ss3840218211, ss3878964283, ss3927685780, ss3984035086, ss3986581990, ss5207839238, ss5315643722, ss5407766938, ss5623958796, ss5624035643, ss5653818158, ss5800065485, ss5838415550, ss5848360209, ss5936554221, ss5945212394, ss5981277815	NC_000012.11:100795698:A:G	NC_000012.12:100401920:A:G	(self)
RCV001649693.2, 77612850, 889795, 28956756, 2940, 91902964, 145806112, 8621149248, ss2192584821, ss3027497973, ss3649909529, ss3694321606, ss3816211829, ss3845706407, ss3972578755, ss4930260455, ss5291982305, ss5486609012, ss5590086915, ss5758065860, ss5813584243, ss5905729269	NC_000012.12:100401920:A:G	NC_000012.12:100401920:A:G	(self)
ss65774997, ss69371683, ss74879812, ss76794487, ss97335169, ss119689242, ss143345095, ss171292312	NT_029419.12:62939004:A:G	NC_000012.12:100401920: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 rs11568544

PMID	Title	Author	Year	Journal
18674745	Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice.	Ruel J et al.	2008	American journal of human genetics

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11568544