Name: rs11309873
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.

rs11309873

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:23181011-23181018 (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: delGG / delG / dupG / dupGG
Variation Type: Indel Insertion and Deletion
Frequency: delG=0.227466 (60208/264690, TOPMED)
delG=0.09946 (1244/12508, ALFA)
delG=0.2120 (1047/4938, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SCNN1G : 2KB Upstream 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	12508	GGGGGGGG=0.87720	GGGGGG=0.00000, GGGGGGG=0.09946, GGGGGGGGG=0.02335, GGGGGGGGGG=0.00000	0.834783	0.029264	0.135953	32
European	Sub	9624	GGGGGGGG=0.8407	GGGGGG=0.0000, GGGGGGG=0.1289, GGGGGGGGG=0.0303, GGGGGGGGGG=0.0000	0.782724	0.038343	0.178933	32
African	Sub	2144	GGGGGGGG=1.0000	GGGGGG=0.0000, GGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	90	GGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
African American	Sub	2054	GGGGGGGG=1.0000	GGGGGG=0.0000, GGGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	92	GGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	68	GGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	GGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	86	GGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	208	GGGGGGGG=1.000	GGGGGG=0.000, GGGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	58	GGGGGGGG=1.00	GGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00	1.0	0.0	0.0	N/A
Other	Sub	296	GGGGGGGG=0.990	GGGGGG=0.000, GGGGGGG=0.010, GGGGGGGGG=0.000, GGGGGGGGGG=0.000	0.986486	0.006757	0.006757	35

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	(G)₈=0.772534	delG=0.227466
Allele Frequency Aggregator	Total	Global	12508	(G)₈=0.87720	delGG=0.00000, delG=0.09946, dupG=0.02335, dupGG=0.00000
Allele Frequency Aggregator	European	Sub	9624	(G)₈=0.8407	delGG=0.0000, delG=0.1289, dupG=0.0303, dupGG=0.0000
Allele Frequency Aggregator	African	Sub	2144	(G)₈=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000
Allele Frequency Aggregator	Other	Sub	296	(G)₈=0.990	delGG=0.000, delG=0.010, dupG=0.000, dupGG=0.000
Allele Frequency Aggregator	Latin American 2	Sub	208	(G)₈=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000
Allele Frequency Aggregator	Asian	Sub	92	(G)₈=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00
Allele Frequency Aggregator	Latin American 1	Sub	86	(G)₈=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(G)₈=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00
1000Genomes	Global	Study-wide	4938	(G)₈=0.7880	delG=0.2120
1000Genomes	African	Sub	1320	(G)₈=0.8652	delG=0.1348
1000Genomes	East Asian	Sub	1000	(G)₈=0.850	delG=0.150
1000Genomes	South Asian	Sub	968	(G)₈=0.782	delG=0.218
1000Genomes	Europe	Sub	964	(G)₈=0.734	delG=0.266
1000Genomes	American	Sub	686	(G)₈=0.633	delG=0.367

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 16	NC_000016.10:g.23181017_23181018del
GRCh38.p14 chr 16	NC_000016.10:g.23181018del
GRCh38.p14 chr 16	NC_000016.10:g.23181018dup
GRCh38.p14 chr 16	NC_000016.10:g.23181017_23181018dup
GRCh37.p13 chr 16	NC_000016.9:g.23192338_23192339del
GRCh37.p13 chr 16	NC_000016.9:g.23192339del
GRCh37.p13 chr 16	NC_000016.9:g.23192339dup
GRCh37.p13 chr 16	NC_000016.9:g.23192338_23192339dup
SCNN1G RefSeqGene	NG_011909.1:g.3299_3300del
SCNN1G RefSeqGene	NG_011909.1:g.3300del
SCNN1G RefSeqGene	NG_011909.1:g.3300dup
SCNN1G RefSeqGene	NG_011909.1:g.3299_3300dup

Gene: SCNN1G, sodium channel epithelial 1 subunit gamma (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
SCNN1G transcript	NM_001039.4:c.	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.

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	(G)₈=	delGG	delG	dupG	dupGG
GRCh38.p14 chr 16	NC_000016.10:g.23181011_23181018=	NC_000016.10:g.23181017_23181018del	NC_000016.10:g.23181018del	NC_000016.10:g.23181018dup	NC_000016.10:g.23181017_23181018dup
GRCh37.p13 chr 16	NC_000016.9:g.23192332_23192339=	NC_000016.9:g.23192338_23192339del	NC_000016.9:g.23192339del	NC_000016.9:g.23192339dup	NC_000016.9:g.23192338_23192339dup
SCNN1G RefSeqGene	NG_011909.1:g.3293_3300=	NG_011909.1:g.3299_3300del	NG_011909.1:g.3300del	NG_011909.1:g.3300dup	NG_011909.1:g.3299_3300dup

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#.

51 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40744641	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss96711886	Feb 05, 2009 (137)
3	BGI	ss104708139	Dec 06, 2013 (138)
4	BUSHMAN	ss193411571	Jul 04, 2010 (132)
5	1000GENOMES	ss327722464	May 09, 2011 (137)
6	1000GENOMES	ss327842854	May 09, 2011 (137)
7	LUNTER	ss552464543	Apr 25, 2013 (138)
8	LUNTER	ss552799990	Apr 25, 2013 (138)
9	LUNTER	ss553593742	Apr 25, 2013 (138)
10	TISHKOFF	ss554817434	Apr 25, 2013 (138)
11	SSMP	ss664306870	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666666789	Apr 25, 2013 (138)
13	1000GENOMES	ss1375671485	Aug 21, 2014 (142)
14	1000GENOMES	ss1375671488	Aug 21, 2014 (142)
15	DDI	ss1536824341	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1708501822	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1708501913	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1710694961	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1710694962	Apr 01, 2015 (144)
20	GENOMED	ss1968240561	Jul 19, 2016 (147)
21	SWEGEN	ss3014241328	Nov 08, 2017 (151)
22	BIOINF_KMB_FNS_UNIBA	ss3645413550	Oct 12, 2018 (152)
23	EVA_DECODE	ss3699028289	Jul 13, 2019 (153)
24	EVA_DECODE	ss3699028290	Jul 13, 2019 (153)
25	ACPOP	ss3741419547	Jul 13, 2019 (153)
26	ACPOP	ss3741419548	Jul 13, 2019 (153)
27	PACBIO	ss3788007527	Jul 13, 2019 (153)
28	PACBIO	ss3792996752	Jul 13, 2019 (153)
29	PACBIO	ss3797881656	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3819094787	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3819094788	Jul 13, 2019 (153)
32	EVA	ss3834520839	Apr 27, 2020 (154)
33	KOGIC	ss3977288749	Apr 27, 2020 (154)
34	KOGIC	ss3977288750	Apr 27, 2020 (154)
35	GNOMAD	ss4298568950	Apr 26, 2021 (155)
36	GNOMAD	ss4298568951	Apr 26, 2021 (155)
37	GNOMAD	ss4298568952	Apr 26, 2021 (155)
38	GNOMAD	ss4298568953	Apr 26, 2021 (155)
39	TOPMED	ss5011006845	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5218917278	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5218917279	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5218917280	Apr 26, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5300493014	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5300493015	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5493946503	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5493946504	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5773540348	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5773540349	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5773540350	Oct 16, 2022 (156)
50	EVA	ss5846239633	Oct 16, 2022 (156)
51	EVA	ss5846239634	Oct 16, 2022 (156)
52	1000Genomes	NC_000016.9 - 23192332	Oct 12, 2018 (152)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 38252402 (NC_000016.9:23192331:G: 913/3854) Row 38252403 (NC_000016.9:23192331::G 194/3854)	-	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 38252402 (NC_000016.9:23192331:G: 913/3854) Row 38252403 (NC_000016.9:23192331::G 194/3854)	-	Oct 12, 2018 (152)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485704860 (NC_000016.10:23181010::G 4483/139070) Row 485704861 (NC_000016.10:23181010::GG 7/139160) Row 485704862 (NC_000016.10:23181010:G: 30471/139118)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485704860 (NC_000016.10:23181010::G 4483/139070) Row 485704861 (NC_000016.10:23181010::GG 7/139160) Row 485704862 (NC_000016.10:23181010:G: 30471/139118)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485704860 (NC_000016.10:23181010::G 4483/139070) Row 485704861 (NC_000016.10:23181010::GG 7/139160) Row 485704862 (NC_000016.10:23181010:G: 30471/139118)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 485704860 (NC_000016.10:23181010::G 4483/139070) Row 485704861 (NC_000016.10:23181010::GG 7/139160) Row 485704862 (NC_000016.10:23181010:G: 30471/139118)...	-	Apr 26, 2021 (155)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 33666750 (NC_000016.10:23181010:G: 260/1832) Row 33666751 (NC_000016.10:23181011::G 16/1832)	-	Apr 27, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 33666750 (NC_000016.10:23181010:G: 260/1832) Row 33666751 (NC_000016.10:23181011::G 16/1832)	-	Apr 27, 2020 (154)
61	Northern Sweden Submission ignored due to conflicting rows: Row 14704412 (NC_000016.9:23192331:G: 173/600) Row 14704413 (NC_000016.9:23192331::G 26/600)	-	Jul 13, 2019 (153)
62	Northern Sweden Submission ignored due to conflicting rows: Row 14704412 (NC_000016.9:23192331:G: 173/600) Row 14704413 (NC_000016.9:23192331::G 26/600)	-	Jul 13, 2019 (153)
63	8.3KJPN Submission ignored due to conflicting rows: Row 76886585 (NC_000016.9:23192331:G: 2424/16760) Row 76886586 (NC_000016.9:23192331::G 132/16760) Row 76886587 (NC_000016.9:23192331::GG 5/16760)	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 76886585 (NC_000016.9:23192331:G: 2424/16760) Row 76886586 (NC_000016.9:23192331::G 132/16760) Row 76886587 (NC_000016.9:23192331::GG 5/16760)	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 76886585 (NC_000016.9:23192331:G: 2424/16760) Row 76886586 (NC_000016.9:23192331::G 132/16760) Row 76886587 (NC_000016.9:23192331::GG 5/16760)	-	Apr 26, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 107377452 (NC_000016.10:23181010:G: 4035/28258) Row 107377453 (NC_000016.10:23181010::G 237/28258) Row 107377454 (NC_000016.10:23181010::GG 9/28258)	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 107377452 (NC_000016.10:23181010:G: 4035/28258) Row 107377453 (NC_000016.10:23181010::G 237/28258) Row 107377454 (NC_000016.10:23181010::GG 9/28258)	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 107377452 (NC_000016.10:23181010:G: 4035/28258) Row 107377453 (NC_000016.10:23181010::G 237/28258) Row 107377454 (NC_000016.10:23181010::GG 9/28258)	-	Oct 16, 2022 (156)
69	TopMed	NC_000016.10 - 23181011	Apr 26, 2021 (155)
70	UK 10K study - Twins Submission ignored due to conflicting rows: Row 38252402 (NC_000016.9:23192331:G: 911/3708) Row 38252403 (NC_000016.9:23192331::G 165/3708)	-	Oct 12, 2018 (152)
71	UK 10K study - Twins Submission ignored due to conflicting rows: Row 38252402 (NC_000016.9:23192331:G: 911/3708) Row 38252403 (NC_000016.9:23192331::G 165/3708)	-	Oct 12, 2018 (152)
72	ALFA	NC_000016.10 - 23181011	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)
rs34258695	May 11, 2012 (137)
rs35680237	May 23, 2006 (127)
rs78040276	May 11, 2012 (137)
rs147157277	May 04, 2012 (137)
rs372014525	May 13, 2013 (138)
rs373987978	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4298568953	NC_000016.10:23181010:GG:	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGG	(self)
2101756030	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGG	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGG	(self)
ss327722464, ss327842854, ss552464543, ss552799990, ss553593742	NC_000016.8:23099832:G:	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	(self)
68914421, ss664306870, ss666666789, ss1375671485, ss1536824341, ss1708501822, ss1708501913, ss1968240561, ss3014241328, ss3741419547, ss3788007527, ss3792996752, ss3797881656, ss3834520839, ss5218917278, ss5846239633	NC_000016.9:23192331:G:	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	(self)
ss554817434	NC_000016.9:23192338:G:	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	(self)
226552506, ss3645413550, ss3699028290, ss3819094787, ss3977288749, ss4298568952, ss5011006845, ss5300493014, ss5493946503, ss5773540348	NC_000016.10:23181010:G:	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	(self)
2101756030	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	(self)
ss104708139	NT_010393.16:23132337:G:	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	(self)
ss40744641, ss96711886	NT_010393.16:23132338:G:	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	(self)
ss193411571	NT_187260.1:4694524:G:	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGG	(self)
ss3741419548, ss5218917279, ss5846239634	NC_000016.9:23192331::G	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGG	(self)
ss1375671488, ss1710694961, ss1710694962	NC_000016.9:23192332::G	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGG	(self)
ss4298568950, ss5300493015, ss5493946504, ss5773540349	NC_000016.10:23181010::G	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGG	(self)
2101756030	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGG	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGG	(self)
ss3699028289, ss3819094788, ss3977288750	NC_000016.10:23181011::G	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGG	(self)
ss5218917280	NC_000016.9:23192331::GG	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGGG	(self)
ss4298568951, ss5773540350	NC_000016.10:23181010::GG	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGGG	(self)
2101756030	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGGG	NC_000016.10:23181010:GGGGGGGG:GGG… NC_000016.10:23181010:GGGGGGGG:GGGGGGGGGG	(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 rs11309873

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

rs11309873