Name: rs11666645
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.

rs11666645

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:1914796 (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: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.307858 (81487/264690, TOPMED)
C=0.204602 (30658/149842, ALFA)
C=0.296123 (41446/139962, GnomAD) (+ 19 more)
C=0.39634 (30707/77476, PAGE_STUDY)
C=0.49455 (13969/28246, 14KJPN)
C=0.49534 (8298/16752, 8.3KJPN)
C=0.3752 (2403/6404, 1000G_30x)
C=0.3728 (1867/5008, 1000G)
C=0.2084 (933/4478, Estonian)
C=0.1689 (651/3854, ALSPAC)
C=0.1624 (602/3708, TWINSUK)
C=0.4672 (1368/2928, KOREAN)
C=0.4054 (767/1892, HapMap)
C=0.4579 (838/1830, Korea1K)
C=0.178 (178/998, GoNL)
C=0.385 (302/784, PRJEB37584)
C=0.212 (127/600, NorthernSweden)
T=0.007 (4/534, MGP)
C=0.233 (111/476, SGDP_PRJ)
C=0.370 (80/216, Qatari)
C=0.22 (11/50, Siberian)
C=0.12 (5/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SCAMP4 : 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	154876	C=0.206475	T=0.793525
European	Sub	135544	C=0.182280	T=0.817720
African	Sub	7328	C=0.4548	T=0.5452
African Others	Sub	270	C=0.474	T=0.526
African American	Sub	7058	C=0.4541	T=0.5459
Asian	Sub	484	C=0.395	T=0.605
East Asian	Sub	418	C=0.392	T=0.608
Other Asian	Sub	66	C=0.41	T=0.59
Latin American 1	Sub	594	C=0.311	T=0.689
Latin American 2	Sub	4974	C=0.4107	T=0.5893
South Asian	Sub	168	C=0.268	T=0.732
Other	Sub	5784	C=0.2548	T=0.7452

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	C=0.307858	T=0.692142
Allele Frequency Aggregator	Total	Global	149842	C=0.204602	T=0.795398
Allele Frequency Aggregator	European	Sub	132450	C=0.182363	T=0.817637
Allele Frequency Aggregator	African	Sub	6186	C=0.4560	T=0.5440
Allele Frequency Aggregator	Other	Sub	4986	C=0.2445	T=0.7555
Allele Frequency Aggregator	Latin American 2	Sub	4974	C=0.4107	T=0.5893
Allele Frequency Aggregator	Latin American 1	Sub	594	C=0.311	T=0.689
Allele Frequency Aggregator	Asian	Sub	484	C=0.395	T=0.605
Allele Frequency Aggregator	South Asian	Sub	168	C=0.268	T=0.732
gnomAD - Genomes	Global	Study-wide	139962	C=0.296123	T=0.703877
gnomAD - Genomes	European	Sub	75832	C=0.19916	T=0.80084
gnomAD - Genomes	African	Sub	41902	C=0.45079	T=0.54921
gnomAD - Genomes	American	Sub	13630	C=0.35649	T=0.64351
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.2298	T=0.7702
gnomAD - Genomes	East Asian	Sub	3124	C=0.3796	T=0.6204
gnomAD - Genomes	Other	Sub	2150	C=0.3000	T=0.7000
The PAGE Study	Global	Study-wide	77476	C=0.39634	T=0.60366
The PAGE Study	AfricanAmerican	Sub	31856	C=0.44959	T=0.55041
The PAGE Study	Mexican	Sub	10666	C=0.37577	T=0.62423
The PAGE Study	Asian	Sub	8186	C=0.4608	T=0.5392
The PAGE Study	PuertoRican	Sub	7832	C=0.3362	T=0.6638
The PAGE Study	NativeHawaiian	Sub	4478	C=0.2336	T=0.7664
The PAGE Study	Cuban	Sub	4186	C=0.2508	T=0.7492
The PAGE Study	Dominican	Sub	3790	C=0.3594	T=0.6406
The PAGE Study	CentralAmerican	Sub	2414	C=0.4209	T=0.5791
The PAGE Study	SouthAmerican	Sub	1970	C=0.4518	T=0.5482
The PAGE Study	NativeAmerican	Sub	1250	C=0.2744	T=0.7256
The PAGE Study	SouthAsian	Sub	848	C=0.312	T=0.688
14KJPN	JAPANESE	Study-wide	28246	C=0.49455	T=0.50545
8.3KJPN	JAPANESE	Study-wide	16752	C=0.49534	T=0.50466
1000Genomes_30x	Global	Study-wide	6404	C=0.3752	T=0.6248
1000Genomes_30x	African	Sub	1786	C=0.5101	T=0.4899
1000Genomes_30x	Europe	Sub	1266	C=0.2299	T=0.7701
1000Genomes_30x	South Asian	Sub	1202	C=0.2987	T=0.7013
1000Genomes_30x	East Asian	Sub	1170	C=0.3658	T=0.6342
1000Genomes_30x	American	Sub	980	C=0.422	T=0.578
1000Genomes	Global	Study-wide	5008	C=0.3728	T=0.6272
1000Genomes	African	Sub	1322	C=0.5023	T=0.4977
1000Genomes	East Asian	Sub	1008	C=0.3681	T=0.6319
1000Genomes	Europe	Sub	1006	C=0.2346	T=0.7654
1000Genomes	South Asian	Sub	978	C=0.308	T=0.692
1000Genomes	American	Sub	694	C=0.425	T=0.575
Genetic variation in the Estonian population	Estonian	Study-wide	4478	C=0.2084	T=0.7916
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.1689	T=0.8311
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.1624	T=0.8376
KOREAN population from KRGDB	KOREAN	Study-wide	2928	C=0.4672	T=0.5328
HapMap	Global	Study-wide	1892	C=0.4054	T=0.5946
HapMap	American	Sub	770	C=0.325	T=0.675
HapMap	African	Sub	692	C=0.512	T=0.488
HapMap	Asian	Sub	254	C=0.457	T=0.543
HapMap	Europe	Sub	176	C=0.267	T=0.733
Korean Genome Project	KOREAN	Study-wide	1830	C=0.4579	T=0.5421
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.178	T=0.822
CNV burdens in cranial meningiomas	Global	Study-wide	784	C=0.385	T=0.615
CNV burdens in cranial meningiomas	CRM	Sub	784	C=0.385	T=0.615
Northern Sweden	ACPOP	Study-wide	600	C=0.212	T=0.788
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	C=0.993	T=0.007
SGDP_PRJ	Global	Study-wide	476	C=0.233	T=0.767
Qatari	Global	Study-wide	216	C=0.370	T=0.630
Siberian	Global	Study-wide	50	C=0.22	T=0.78
The Danish reference pan genome	Danish	Study-wide	40	C=0.12	T=0.88

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 19	NC_000019.10:g.1914796C>T
GRCh37.p13 chr 19	NC_000019.9:g.1914795C>T
ADAT3 RefSeqGene	NG_051211.1:g.14583C>T

Gene: SCAMP4, secretory carrier membrane protein 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SCAMP4 transcript variant 2	NM_001329539.2:c.-125-289… NM_001329539.2:c.-125-2898C>T	N/A	Intron Variant
SCAMP4 transcript variant 3	NM_001329540.2:c.-41-183C… NM_001329540.2:c.-41-183C>T	N/A	Intron Variant
SCAMP4 transcript variant 1	NM_079834.4:c.-41-183C>T	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	C=	T
GRCh38.p14 chr 19	NC_000019.10:g.1914796=	NC_000019.10:g.1914796C>T
GRCh37.p13 chr 19	NC_000019.9:g.1914795=	NC_000019.9:g.1914795C>T
ADAT3 RefSeqGene	NG_051211.1:g.14583=	NG_051211.1:g.14583C>T
SCAMP4 transcript variant 2	NM_001329539.2:c.-125-2898=	NM_001329539.2:c.-125-2898C>T
SCAMP4 transcript variant 3	NM_001329540.2:c.-41-183=	NM_001329540.2:c.-41-183C>T
SCAMP4 transcript	NM_079834.2:c.-41-183=	NM_079834.2:c.-41-183C>T
SCAMP4 transcript variant 1	NM_079834.4:c.-41-183=	NM_079834.4:c.-41-183C>T
SCAMP4 transcript variant X1	XM_005259481.1:c.-41-183=	XM_005259481.1:c.-41-183C>T
SCAMP4 transcript variant X2	XM_005259482.1:c.-41-183=	XM_005259482.1:c.-41-183C>T

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#.

120 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CSHL-HAPMAP	ss16788870	Feb 28, 2004 (120)
2	SSAHASNP	ss21531758	Apr 05, 2004 (121)
3	ABI	ss44197223	Mar 13, 2006 (126)
4	ILLUMINA	ss74998640	Dec 07, 2007 (129)
5	HGSV	ss77468465	Dec 07, 2007 (129)
6	BCMHGSC_JDW	ss90880769	Mar 24, 2008 (129)
7	HUMANGENOME_JCVI	ss96285503	Feb 06, 2009 (130)
8	BGI	ss103417881	Dec 01, 2009 (131)
9	1000GENOMES	ss110981488	Jan 25, 2009 (130)
10	1000GENOMES	ss114739655	Jan 25, 2009 (130)
11	KRIBB_YJKIM	ss119701694	Dec 01, 2009 (131)
12	ENSEMBL	ss136311311	Dec 01, 2009 (131)
13	ENSEMBL	ss137514522	Dec 01, 2009 (131)
14	GMI	ss155524983	Dec 01, 2009 (131)
15	ILLUMINA	ss159991930	Dec 01, 2009 (131)
16	COMPLETE_GENOMICS	ss167655502	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss168864759	Jul 04, 2010 (132)
18	COMPLETE_GENOMICS	ss171386383	Jul 04, 2010 (132)
19	ILLUMINA	ss171415007	Jul 04, 2010 (132)
20	BUSHMAN	ss203587114	Jul 04, 2010 (132)
21	BCM-HGSC-SUB	ss208431029	Jul 04, 2010 (132)
22	1000GENOMES	ss228008499	Jul 14, 2010 (132)
23	1000GENOMES	ss237578111	Jul 15, 2010 (132)
24	1000GENOMES	ss243805395	Jul 15, 2010 (132)
25	BL	ss255432890	May 09, 2011 (134)
26	GMI	ss283097590	May 04, 2012 (137)
27	GMI	ss287333526	Apr 25, 2013 (138)
28	PJP	ss292173414	May 09, 2011 (134)
29	ILLUMINA	ss479558760	May 04, 2012 (137)
30	ILLUMINA	ss479563022	May 04, 2012 (137)
31	ILLUMINA	ss480033489	Sep 08, 2015 (146)
32	ILLUMINA	ss484578266	May 04, 2012 (137)
33	TISHKOFF	ss565808392	Apr 25, 2013 (138)
34	SSMP	ss661660590	Apr 25, 2013 (138)
35	ILLUMINA	ss782735897	Sep 08, 2015 (146)
36	ILLUMINA	ss831987728	Sep 08, 2015 (146)
37	EVA-GONL	ss994012327	Aug 21, 2014 (142)
38	JMKIDD_LAB	ss1081711432	Aug 21, 2014 (142)
39	1000GENOMES	ss1362066593	Aug 21, 2014 (142)
40	DDI	ss1428311575	Apr 01, 2015 (144)
41	EVA_GENOME_DK	ss1578525592	Apr 01, 2015 (144)
42	EVA_UK10K_ALSPAC	ss1637431982	Apr 01, 2015 (144)
43	EVA_UK10K_TWINSUK	ss1680426015	Apr 01, 2015 (144)
44	EVA_DECODE	ss1698075418	Apr 01, 2015 (144)
45	EVA_MGP	ss1711491758	Apr 01, 2015 (144)
46	EVA_SVP	ss1713646736	Apr 01, 2015 (144)
47	ILLUMINA	ss1752277669	Sep 08, 2015 (146)
48	HAMMER_LAB	ss1809173046	Sep 08, 2015 (146)
49	WEILL_CORNELL_DGM	ss1937489707	Feb 12, 2016 (147)
50	ILLUMINA	ss1946519402	Feb 12, 2016 (147)
51	ILLUMINA	ss1959828023	Feb 12, 2016 (147)
52	GENOMED	ss1968592787	Jul 19, 2016 (147)
53	JJLAB	ss2029519856	Sep 14, 2016 (149)
54	USC_VALOUEV	ss2158032398	Dec 20, 2016 (150)
55	HUMAN_LONGEVITY	ss2223712713	Dec 20, 2016 (150)
56	SYSTEMSBIOZJU	ss2629258701	Nov 08, 2017 (151)
57	ILLUMINA	ss2633509042	Nov 08, 2017 (151)
58	ILLUMINA	ss2635080838	Nov 08, 2017 (151)
59	GRF	ss2702636003	Nov 08, 2017 (151)
60	GNOMAD	ss2959614261	Nov 08, 2017 (151)
61	SWEGEN	ss3016962718	Nov 08, 2017 (151)
62	ILLUMINA	ss3021868623	Nov 08, 2017 (151)
63	BIOINF_KMB_FNS_UNIBA	ss3028592492	Nov 08, 2017 (151)
64	CSHL	ss3352160617	Nov 08, 2017 (151)
65	ILLUMINA	ss3625730460	Oct 12, 2018 (152)
66	ILLUMINA	ss3633172399	Oct 12, 2018 (152)
67	ILLUMINA	ss3633881788	Oct 12, 2018 (152)
68	ILLUMINA	ss3634718535	Oct 12, 2018 (152)
69	ILLUMINA	ss3635568853	Oct 12, 2018 (152)
70	ILLUMINA	ss3636409187	Oct 12, 2018 (152)
71	ILLUMINA	ss3637320520	Oct 12, 2018 (152)
72	ILLUMINA	ss3638211253	Oct 12, 2018 (152)
73	ILLUMINA	ss3640425843	Oct 12, 2018 (152)
74	ILLUMINA	ss3643185906	Oct 12, 2018 (152)
75	ILLUMINA	ss3644712025	Oct 12, 2018 (152)
76	URBANLAB	ss3650852222	Oct 12, 2018 (152)
77	ILLUMINA	ss3652292599	Oct 12, 2018 (152)
78	EGCUT_WGS	ss3683811823	Jul 13, 2019 (153)
79	EVA_DECODE	ss3702187899	Jul 13, 2019 (153)
80	ACPOP	ss3742787795	Jul 13, 2019 (153)
81	ILLUMINA	ss3744162688	Jul 13, 2019 (153)
82	ILLUMINA	ss3745018607	Jul 13, 2019 (153)
83	EVA	ss3755723349	Jul 13, 2019 (153)
84	PAGE_CC	ss3771989502	Jul 13, 2019 (153)
85	ILLUMINA	ss3772516024	Jul 13, 2019 (153)
86	PACBIO	ss3788446672	Jul 13, 2019 (153)
87	PACBIO	ss3793369999	Jul 13, 2019 (153)
88	PACBIO	ss3798256542	Jul 13, 2019 (153)
89	KHV_HUMAN_GENOMES	ss3820977471	Jul 13, 2019 (153)
90	EVA	ss3835311012	Apr 27, 2020 (154)
91	EVA	ss3841278099	Apr 27, 2020 (154)
92	EVA	ss3846781936	Apr 27, 2020 (154)
93	SGDP_PRJ	ss3887595051	Apr 27, 2020 (154)
94	KRGDB	ss3937523150	Apr 27, 2020 (154)
95	KOGIC	ss3980651708	Apr 27, 2020 (154)
96	FSA-LAB	ss3984137703	Apr 26, 2021 (155)
97	EVA	ss3984737248	Apr 26, 2021 (155)
98	EVA	ss3986766664	Apr 26, 2021 (155)
99	EVA	ss4017812067	Apr 26, 2021 (155)
100	TOPMED	ss5065642644	Apr 26, 2021 (155)
101	TOMMO_GENOMICS	ss5226364992	Apr 26, 2021 (155)
102	EVA	ss5237244015	Apr 26, 2021 (155)
103	1000G_HIGH_COVERAGE	ss5306217228	Oct 16, 2022 (156)
104	EVA	ss5315956067	Oct 16, 2022 (156)
105	EVA	ss5433105079	Oct 16, 2022 (156)
106	HUGCELL_USP	ss5498888489	Oct 16, 2022 (156)
107	EVA	ss5512027911	Oct 16, 2022 (156)
108	1000G_HIGH_COVERAGE	ss5611511598	Oct 16, 2022 (156)
109	EVA	ss5624082670	Oct 16, 2022 (156)
110	SANFORD_IMAGENETICS	ss5661827705	Oct 16, 2022 (156)
111	TOMMO_GENOMICS	ss5784511239	Oct 16, 2022 (156)
112	EVA	ss5800001980	Oct 16, 2022 (156)
113	YY_MCH	ss5817338983	Oct 16, 2022 (156)
114	EVA	ss5840149086	Oct 16, 2022 (156)
115	EVA	ss5847830772	Oct 16, 2022 (156)
116	EVA	ss5848473951	Oct 16, 2022 (156)
117	EVA	ss5852174732	Oct 16, 2022 (156)
118	EVA	ss5927013320	Oct 16, 2022 (156)
119	EVA	ss5936571168	Oct 16, 2022 (156)
120	EVA	ss5953258816	Oct 16, 2022 (156)
121	1000Genomes	NC_000019.9 - 1914795	Oct 12, 2018 (152)
122	1000Genomes_30x	NC_000019.10 - 1914796	Oct 16, 2022 (156)
123	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 1914795	Oct 12, 2018 (152)
124	Genetic variation in the Estonian population	NC_000019.9 - 1914795	Oct 12, 2018 (152)
125	The Danish reference pan genome	NC_000019.9 - 1914795	Apr 27, 2020 (154)
126	gnomAD - Genomes	NC_000019.10 - 1914796	Apr 26, 2021 (155)
127	Genome of the Netherlands Release 5	NC_000019.9 - 1914795	Apr 27, 2020 (154)
128	HapMap	NC_000019.10 - 1914796	Apr 27, 2020 (154)
129	KOREAN population from KRGDB	NC_000019.9 - 1914795	Apr 27, 2020 (154)
130	Korean Genome Project	NC_000019.10 - 1914796	Apr 27, 2020 (154)
131	Medical Genome Project healthy controls from Spanish population	NC_000019.9 - 1914795	Apr 27, 2020 (154)
132	Northern Sweden	NC_000019.9 - 1914795	Jul 13, 2019 (153)
133	The PAGE Study	NC_000019.10 - 1914796	Jul 13, 2019 (153)
134	CNV burdens in cranial meningiomas	NC_000019.9 - 1914795	Apr 26, 2021 (155)
135	Qatari	NC_000019.9 - 1914795	Apr 27, 2020 (154)
136	SGDP_PRJ	NC_000019.9 - 1914795	Apr 27, 2020 (154)
137	Siberian	NC_000019.9 - 1914795	Apr 27, 2020 (154)
138	8.3KJPN	NC_000019.9 - 1914795	Apr 26, 2021 (155)
139	14KJPN	NC_000019.10 - 1914796	Oct 16, 2022 (156)
140	TopMed	NC_000019.10 - 1914796	Apr 26, 2021 (155)
141	UK 10K study - Twins	NC_000019.9 - 1914795	Oct 12, 2018 (152)
142	ALFA	NC_000019.10 - 1914796	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
ss77468465, ss90880769, ss110981488, ss114739655, ss167655502, ss168864759, ss171386383, ss203587114, ss208431029, ss255432890, ss283097590, ss287333526, ss292173414, ss479558760, ss1698075418, ss1713646736, ss2635080838, ss3643185906	NC_000019.8:1865794:C:T	NC_000019.10:1914795:C:T	(self)
75433040, 41811060, 29550071, 4712737, 18627998, 44700544, 607518, 16072660, 286800, 19531629, 39612031, 10548752, 84334299, 41811060, ss228008499, ss237578111, ss243805395, ss479563022, ss480033489, ss484578266, ss565808392, ss661660590, ss782735897, ss831987728, ss994012327, ss1081711432, ss1362066593, ss1428311575, ss1578525592, ss1637431982, ss1680426015, ss1711491758, ss1752277669, ss1809173046, ss1937489707, ss1946519402, ss1959828023, ss1968592787, ss2029519856, ss2158032398, ss2629258701, ss2633509042, ss2702636003, ss2959614261, ss3016962718, ss3021868623, ss3352160617, ss3625730460, ss3633172399, ss3633881788, ss3634718535, ss3635568853, ss3636409187, ss3637320520, ss3638211253, ss3640425843, ss3644712025, ss3652292599, ss3683811823, ss3742787795, ss3744162688, ss3745018607, ss3755723349, ss3772516024, ss3788446672, ss3793369999, ss3798256542, ss3835311012, ss3841278099, ss3887595051, ss3937523150, ss3984137703, ss3984737248, ss3986766664, ss4017812067, ss5226364992, ss5315956067, ss5433105079, ss5512027911, ss5624082670, ss5661827705, ss5800001980, ss5840149086, ss5847830772, ss5848473951, ss5936571168, ss5953258816	NC_000019.9:1914794:C:T	NC_000019.10:1914795:C:T	(self)
99037533, 531970746, 1658776, 37029709, 1210971, 118348343, 281188308, 9718710884, ss2223712713, ss3028592492, ss3650852222, ss3702187899, ss3771989502, ss3820977471, ss3846781936, ss3980651708, ss5065642644, ss5237244015, ss5306217228, ss5498888489, ss5611511598, ss5784511239, ss5817338983, ss5852174732, ss5927013320	NC_000019.10:1914795:C:T	NC_000019.10:1914795:C:T	(self)
ss16788870, ss21531758, ss44197223, ss74998640, ss96285503, ss103417881, ss119701694, ss136311311, ss137514522, ss155524983, ss159991930, ss171415007	NT_011255.14:1854794:C:T	NC_000019.10:1914795:C:T	(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 rs11666645

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

rs11666645