Name: rs11304207
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.

rs11304207

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:78246748-78246757 (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: delAA / delA / dupA / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.4623 (3209/6942, ALFA)
delA=0.4443 (2225/5008, 1000G)
(A)₁₀=0.2839 (1270/4474, Estonian) (+ 5 more)
(A)₁₀=0.3230 (1245/3854, ALSPAC)
(A)₁₀=0.3077 (1141/3708, TWINSUK)
(A)₁₀=0.315 (314/998, GoNL)
(A)₁₀=0.312 (187/600, NorthernSweden)
(A)₁₀=0.28 (11/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FRAS1 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6942	AAAAAAAAAA=0.5377	AAAAAAAA=0.0000, AAAAAAAAA=0.4623, AAAAAAAAAAA=0.0000	0.407952	0.332469	0.259579	32
European	Sub	5306	AAAAAAAAAA=0.3963	AAAAAAAA=0.0000, AAAAAAAAA=0.6037, AAAAAAAAAAA=0.0000	0.226913	0.434225	0.338862	32
African	Sub	1326	AAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	66	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1260	AAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	46	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	20	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	96	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	30	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	118	AAAAAAAAAA=0.949	AAAAAAAA=0.000, AAAAAAAAA=0.051, AAAAAAAAAAA=0.000	0.932203	0.033898	0.033898	14

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
Allele Frequency Aggregator	Total	Global	6942	(A)₁₀=0.5377	delAA=0.0000, delA=0.4623, dupA=0.0000
Allele Frequency Aggregator	European	Sub	5306	(A)₁₀=0.3963	delAA=0.0000, delA=0.6037, dupA=0.0000
Allele Frequency Aggregator	African	Sub	1326	(A)₁₀=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	Other	Sub	118	(A)₁₀=0.949	delAA=0.000, delA=0.051, dupA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	96	(A)₁₀=1.00	delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Asian	Sub	46	(A)₁₀=1.00	delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(A)₁₀=1.00	delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(A)₁₀=1.00	delAA=0.00, delA=0.00, dupA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₀=0.5557	delA=0.4443
1000Genomes	African	Sub	1322	(A)₁₀=0.7307	delA=0.2693
1000Genomes	East Asian	Sub	1008	(A)₁₀=0.6210	delA=0.3790
1000Genomes	Europe	Sub	1006	(A)₁₀=0.3340	delA=0.6660
1000Genomes	South Asian	Sub	978	(A)₁₀=0.610	delA=0.390
1000Genomes	American	Sub	694	(A)₁₀=0.372	delA=0.628
Genetic variation in the Estonian population	Estonian	Study-wide	4474	(A)₁₀=0.2839	delA=0.7161
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₀=0.3230	delA=0.6770
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(A)₁₀=0.3077	delA=0.6923
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	(A)₁₀=0.315	delA=0.685
Northern Sweden	ACPOP	Study-wide	600	(A)₁₀=0.312	delA=0.688
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₀=0.28	delA=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 4	NC_000004.12:g.78246756_78246757del
GRCh38.p14 chr 4	NC_000004.12:g.78246757del
GRCh38.p14 chr 4	NC_000004.12:g.78246757dup
GRCh38.p14 chr 4	NC_000004.12:g.78246752_78246757dup
GRCh37.p13 chr 4	NC_000004.11:g.79167910_79167911del
GRCh37.p13 chr 4	NC_000004.11:g.79167911del
GRCh37.p13 chr 4	NC_000004.11:g.79167911dup
GRCh37.p13 chr 4	NC_000004.11:g.79167906_79167911dup
FRAS1 RefSeqGene	NG_015812.2:g.194187_194188del
FRAS1 RefSeqGene	NG_015812.2:g.194188del
FRAS1 RefSeqGene	NG_015812.2:g.194188dup
FRAS1 RefSeqGene	NG_015812.2:g.194183_194188dup

Gene: FRAS1, Fraser extracellular matrix complex subunit 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FRAS1 transcript variant 2	NM_001166133.2:c.309+1431… NM_001166133.2:c.309+1431_309+1432del	N/A	Intron Variant
FRAS1 transcript variant 1	NM_025074.7:c.309+1431_30… NM_025074.7:c.309+1431_309+1432del	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	(A)₁₀=	delAA	delA	dupA	dup(A)₆
GRCh38.p14 chr 4	NC_000004.12:g.78246748_78246757=	NC_000004.12:g.78246756_78246757del	NC_000004.12:g.78246757del	NC_000004.12:g.78246757dup	NC_000004.12:g.78246752_78246757dup
GRCh37.p13 chr 4	NC_000004.11:g.79167902_79167911=	NC_000004.11:g.79167910_79167911del	NC_000004.11:g.79167911del	NC_000004.11:g.79167911dup	NC_000004.11:g.79167906_79167911dup
FRAS1 RefSeqGene	NG_015812.2:g.194179_194188=	NG_015812.2:g.194187_194188del	NG_015812.2:g.194188del	NG_015812.2:g.194188dup	NG_015812.2:g.194183_194188dup
FRAS1 transcript variant 2	NM_001166133.1:c.309+1423=	NM_001166133.1:c.309+1431_309+1432del	NM_001166133.1:c.309+1432del	NM_001166133.1:c.309+1432dup	NM_001166133.1:c.309+1427_309+1432dup
FRAS1 transcript variant 2	NM_001166133.2:c.309+1423=	NM_001166133.2:c.309+1431_309+1432del	NM_001166133.2:c.309+1432del	NM_001166133.2:c.309+1432dup	NM_001166133.2:c.309+1427_309+1432dup
FRAS1 transcript variant 1	NM_025074.6:c.309+1423=	NM_025074.6:c.309+1431_309+1432del	NM_025074.6:c.309+1432del	NM_025074.6:c.309+1432dup	NM_025074.6:c.309+1427_309+1432dup
FRAS1 transcript variant 1	NM_025074.7:c.309+1423=	NM_025074.7:c.309+1431_309+1432del	NM_025074.7:c.309+1432del	NM_025074.7:c.309+1432dup	NM_025074.7:c.309+1427_309+1432dup

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#.

63 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42170232	Mar 15, 2006 (137)
2	HUMANGENOME_JCVI	ss95359885	Dec 05, 2013 (138)
3	BGI	ss104751246	Dec 01, 2009 (137)
4	BUSHMAN	ss193745372	Jul 04, 2010 (137)
5	BL	ss256019502	May 09, 2011 (137)
6	GMI	ss287750921	May 09, 2011 (137)
7	GMI	ss288545286	May 04, 2012 (137)
8	PJP	ss295173348	May 09, 2011 (134)
9	1000GENOMES	ss326537697	May 09, 2011 (137)
10	1000GENOMES	ss326569287	May 09, 2011 (137)
11	1000GENOMES	ss326737404	May 09, 2011 (137)
12	LUNTER	ss551379920	Apr 25, 2013 (138)
13	LUNTER	ss551501665	Apr 25, 2013 (138)
14	LUNTER	ss553138947	Apr 25, 2013 (138)
15	TISHKOFF	ss554099397	Apr 25, 2013 (138)
16	SSMP	ss663531040	Apr 01, 2015 (144)
17	BILGI_BIOE	ss666265196	Apr 25, 2013 (138)
18	EVA-GONL	ss980290839	Aug 21, 2014 (142)
19	1000GENOMES	ss1372355485	Aug 21, 2014 (142)
20	DDI	ss1536414087	Apr 01, 2015 (144)
21	EVA_GENOME_DK	ss1576269815	Apr 01, 2015 (144)
22	EVA_UK10K_ALSPAC	ss1704221865	Apr 01, 2015 (144)
23	EVA_UK10K_TWINSUK	ss1704222075	Apr 01, 2015 (144)
24	HAMMER_LAB	ss1801706718	Sep 08, 2015 (146)
25	JJLAB	ss2030608523	Sep 14, 2016 (149)
26	SYSTEMSBIOZJU	ss2625677780	Nov 08, 2017 (151)
27	SWEGEN	ss2994971928	Nov 08, 2017 (151)
28	MCHAISSO	ss3064109093	Nov 08, 2017 (151)
29	MCHAISSO	ss3064976143	Nov 08, 2017 (151)
30	MCHAISSO	ss3065958118	Nov 08, 2017 (151)
31	BEROUKHIMLAB	ss3644158133	Oct 12, 2018 (152)
32	BIOINF_KMB_FNS_UNIBA	ss3645805737	Oct 12, 2018 (152)
33	URBANLAB	ss3647770478	Oct 12, 2018 (152)
34	EGCUT_WGS	ss3662855775	Jul 13, 2019 (153)
35	EVA_DECODE	ss3712372281	Jul 13, 2019 (153)
36	EVA_DECODE	ss3712372282	Jul 13, 2019 (153)
37	EVA_DECODE	ss3712372283	Jul 13, 2019 (153)
38	ACPOP	ss3731295886	Jul 13, 2019 (153)
39	PACBIO	ss3784763845	Jul 13, 2019 (153)
40	PACBIO	ss3790214907	Jul 13, 2019 (153)
41	PACBIO	ss3795090257	Jul 13, 2019 (153)
42	KHV_HUMAN_GENOMES	ss3805139828	Jul 13, 2019 (153)
43	EVA	ss3828628607	Apr 26, 2020 (154)
44	EVA	ss3837755845	Apr 26, 2020 (154)
45	EVA	ss3843193368	Apr 26, 2020 (154)
46	GNOMAD	ss4114168074	Apr 26, 2021 (155)
47	GNOMAD	ss4114168075	Apr 26, 2021 (155)
48	GNOMAD	ss4114168076	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5166442832	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5166442833	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5166442834	Apr 26, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5259780115	Oct 13, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5259780116	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5458475907	Oct 13, 2022 (156)
55	HUGCELL_USP	ss5458475908	Oct 13, 2022 (156)
56	EVA	ss5507583055	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5700991911	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5700991912	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5700991913	Oct 13, 2022 (156)
60	EVA	ss5844221445	Oct 13, 2022 (156)
61	EVA	ss5854296642	Oct 13, 2022 (156)
62	EVA	ss5864099378	Oct 13, 2022 (156)
63	EVA	ss5963750771	Oct 13, 2022 (156)
64	1000Genomes	NC_000004.11 - 79167902	Oct 12, 2018 (152)
65	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 79167902	Oct 12, 2018 (152)
66	Genetic variation in the Estonian population	NC_000004.11 - 79167902	Oct 12, 2018 (152)
67	The Danish reference pan genome	NC_000004.11 - 79167902	Apr 26, 2020 (154)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 154564603 (NC_000004.12:78246747::A 10/138554) Row 154564604 (NC_000004.12:78246747:A: 76850/138476) Row 154564605 (NC_000004.12:78246747:AA: 10/138570)	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 154564603 (NC_000004.12:78246747::A 10/138554) Row 154564604 (NC_000004.12:78246747:A: 76850/138476) Row 154564605 (NC_000004.12:78246747:AA: 10/138570)	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 154564603 (NC_000004.12:78246747::A 10/138554) Row 154564604 (NC_000004.12:78246747:A: 76850/138476) Row 154564605 (NC_000004.12:78246747:AA: 10/138570)	-	Apr 26, 2021 (155)
71	Genome of the Netherlands Release 5	NC_000004.11 - 79167902	Apr 26, 2020 (154)
72	Northern Sweden	NC_000004.11 - 79167902	Jul 13, 2019 (153)
73	8.3KJPN Submission ignored due to conflicting rows: Row 24412139 (NC_000004.11:79167901:A: 6196/16760) Row 24412140 (NC_000004.11:79167901:AA: 5/16760) Row 24412141 (NC_000004.11:79167901::A 9/16760)	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 24412139 (NC_000004.11:79167901:A: 6196/16760) Row 24412140 (NC_000004.11:79167901:AA: 5/16760) Row 24412141 (NC_000004.11:79167901::A 9/16760)	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 24412139 (NC_000004.11:79167901:A: 6196/16760) Row 24412140 (NC_000004.11:79167901:AA: 5/16760) Row 24412141 (NC_000004.11:79167901::A 9/16760)	-	Apr 26, 2021 (155)
76	14KJPN Submission ignored due to conflicting rows: Row 34829015 (NC_000004.12:78246747:A: 10495/28258) Row 34829016 (NC_000004.12:78246747:AA: 9/28258) Row 34829017 (NC_000004.12:78246747::A 10/28258)	-	Oct 13, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 34829015 (NC_000004.12:78246747:A: 10495/28258) Row 34829016 (NC_000004.12:78246747:AA: 9/28258) Row 34829017 (NC_000004.12:78246747::A 10/28258)	-	Oct 13, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 34829015 (NC_000004.12:78246747:A: 10495/28258) Row 34829016 (NC_000004.12:78246747:AA: 9/28258) Row 34829017 (NC_000004.12:78246747::A 10/28258)	-	Oct 13, 2022 (156)
79	UK 10K study - Twins	NC_000004.11 - 79167902	Oct 12, 2018 (152)
80	ALFA	NC_000004.12 - 78246748	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)
rs35465466	May 11, 2012 (137)
rs77042480	May 11, 2012 (137)
rs149380063	May 04, 2012 (137)
rs372172013	May 13, 2013 (138)
rs375985110	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5166442833	NC_000004.11:79167901:AA:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAA	(self)
ss4114168076, ss5700991912	NC_000004.12:78246747:AA:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAA	(self)
4625300203	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAA	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAA	(self)
ss256019502, ss288545286, ss326537697, ss326569287, ss326737404, ss551379920, ss551501665, ss553138947	NC_000004.10:79386925:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
ss295173348	NC_000004.10:79386934:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
21820728, 12131770, 8594023, 920893, 5358132, 4580751, 12131770, ss663531040, ss666265196, ss980290839, ss1372355485, ss1536414087, ss1576269815, ss1704221865, ss1704222075, ss1801706718, ss2030608523, ss2625677780, ss2994971928, ss3644158133, ss3662855775, ss3731295886, ss3784763845, ss3790214907, ss3795090257, ss3828628607, ss3837755845, ss5166442832, ss5844221445, ss5963750771	NC_000004.11:79167901:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
ss554099397	NC_000004.11:79167910:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
ss3064109093, ss3064976143, ss3065958118, ss3645805737, ss3647770478, ss3712372283, ss3805139828, ss3843193368, ss4114168075, ss5259780115, ss5458475907, ss5700991911, ss5854296642, ss5864099378	NC_000004.12:78246747:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
4625300203	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
ss42170232, ss287750921	NT_016354.19:3715622:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
ss104751246	NT_016354.19:3715630:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
ss95359885	NT_016354.19:3715631:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
ss193745372	NT_016354.20:19325366:A:	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAA	(self)
ss5166442834, ss5507583055	NC_000004.11:79167901::A	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss4114168074, ss5259780116, ss5458475908, ss5700991913	NC_000004.12:78246747::A	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAAAA	(self)
4625300203	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAAAA	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3712372282	NC_000004.12:78246748::A	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3712372281	NC_000004.12:78246748::AAAAAA	NC_000004.12:78246747:AAAAAAAAAA:A… NC_000004.12:78246747:AAAAAAAAAA:AAAAAAAAAAAAAAAA	(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 rs11304207

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11304207