Name: rs911115
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.

rs911115

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:18525972 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.092678 (24531/264690, TOPMED)
T=0.028513 (7159/251082, GnomAD_exome)
T=0.086308 (12099/140184, GnomAD) (+ 22 more)
T=0.032848 (3985/121316, ExAC)
T=0.02275 (643/28258, 14KJPN)
T=0.04000 (1130/28252, ALFA)
T=0.02273 (381/16760, 8.3KJPN)
T=0.09219 (1199/13006, GO-ESP)
T=0.1049 (672/6404, 1000G_30x)
T=0.0996 (499/5008, 1000G)
T=0.0011 (5/4480, Estonian)
T=0.0036 (14/3854, ALSPAC)
T=0.0040 (15/3708, TWINSUK)
T=0.0109 (32/2930, KOREAN)
T=0.0169 (31/1832, Korea1K)
T=0.003 (3/998, GoNL)
T=0.008 (5/614, Vietnamese)
T=0.002 (1/600, NorthernSweden)
T=0.045 (25/552, SGDP_PRJ)
T=0.066 (35/534, MGP)
T=0.003 (1/304, FINRISK)
T=0.106 (23/216, Qatari)
T=0.025 (5/198, HapMap)
T=0.00 (0/56, Siberian)
T=0.00 (0/40, GENOME_DK)

Clinical Significance: Reported in ClinVar
Gene : Consequence: SEC23B : 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	28252	T=0.04000	C=0.96000
European	Sub	20398	T=0.00657	C=0.99343
African	Sub	3578	T=0.2387	C=0.7613
African Others	Sub	122	T=0.230	C=0.770
African American	Sub	3456	T=0.2390	C=0.7610
Asian	Sub	172	T=0.000	C=1.000
East Asian	Sub	114	T=0.000	C=1.000
Other Asian	Sub	58	T=0.00	C=1.00
Latin American 1	Sub	154	T=0.065	C=0.935
Latin American 2	Sub	616	T=0.028	C=0.972
South Asian	Sub	98	T=0.04	C=0.96
Other	Sub	3236	T=0.0343	C=0.9657

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=0.092678	C=0.907322
gnomAD - Exomes	Global	Study-wide	251082	T=0.028513	C=0.971487
gnomAD - Exomes	European	Sub	135094	T=0.003383	C=0.996617
gnomAD - Exomes	Asian	Sub	48994	T=0.02672	C=0.97328
gnomAD - Exomes	American	Sub	34572	T=0.02042	C=0.97958
gnomAD - Exomes	African	Sub	16226	T=0.26951	C=0.73049
gnomAD - Exomes	Ashkenazi Jewish	Sub	10074	T=0.01856	C=0.98144
gnomAD - Exomes	Other	Sub	6122	T=0.0207	C=0.9793
gnomAD - Genomes	Global	Study-wide	140184	T=0.086308	C=0.913692
gnomAD - Genomes	European	Sub	75960	T=0.00355	C=0.99645
gnomAD - Genomes	African	Sub	41960	T=0.26368	C=0.73632
gnomAD - Genomes	American	Sub	13656	T=0.03940	C=0.96060
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.0168	C=0.9832
gnomAD - Genomes	East Asian	Sub	3134	T=0.0073	C=0.9927
gnomAD - Genomes	Other	Sub	2150	T=0.0688	C=0.9312
ExAC	Global	Study-wide	121316	T=0.032848	C=0.967152
ExAC	Europe	Sub	73310	T=0.00401	C=0.99599
ExAC	Asian	Sub	25150	T=0.02636	C=0.97364
ExAC	American	Sub	11566	T=0.01859	C=0.98141
ExAC	African	Sub	10382	T=0.26883	C=0.73117
ExAC	Other	Sub	908	T=0.024	C=0.976
14KJPN	JAPANESE	Study-wide	28258	T=0.02275	C=0.97725
Allele Frequency Aggregator	Total	Global	28252	T=0.04000	C=0.96000
Allele Frequency Aggregator	European	Sub	20398	T=0.00657	C=0.99343
Allele Frequency Aggregator	African	Sub	3578	T=0.2387	C=0.7613
Allele Frequency Aggregator	Other	Sub	3236	T=0.0343	C=0.9657
Allele Frequency Aggregator	Latin American 2	Sub	616	T=0.028	C=0.972
Allele Frequency Aggregator	Asian	Sub	172	T=0.000	C=1.000
Allele Frequency Aggregator	Latin American 1	Sub	154	T=0.065	C=0.935
Allele Frequency Aggregator	South Asian	Sub	98	T=0.04	C=0.96
8.3KJPN	JAPANESE	Study-wide	16760	T=0.02273	C=0.97727
GO Exome Sequencing Project	Global	Study-wide	13006	T=0.09219	C=0.90781
GO Exome Sequencing Project	European American	Sub	8600	T=0.0049	C=0.9951
GO Exome Sequencing Project	African American	Sub	4406	T=0.2626	C=0.7374
1000Genomes_30x	Global	Study-wide	6404	T=0.1049	C=0.8951
1000Genomes_30x	African	Sub	1786	T=0.3130	C=0.6870
1000Genomes_30x	Europe	Sub	1266	T=0.0032	C=0.9968
1000Genomes_30x	South Asian	Sub	1202	T=0.0541	C=0.9459
1000Genomes_30x	East Asian	Sub	1170	T=0.0103	C=0.9897
1000Genomes_30x	American	Sub	980	T=0.033	C=0.967
1000Genomes	Global	Study-wide	5008	T=0.0996	C=0.9004
1000Genomes	African	Sub	1322	T=0.3116	C=0.6884
1000Genomes	East Asian	Sub	1008	T=0.0109	C=0.9891
1000Genomes	Europe	Sub	1006	T=0.0030	C=0.9970
1000Genomes	South Asian	Sub	978	T=0.050	C=0.950
1000Genomes	American	Sub	694	T=0.035	C=0.965
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.0011	C=0.9989
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.0036	C=0.9964
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.0040	C=0.9960
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.0109	C=0.9891
Korean Genome Project	KOREAN	Study-wide	1832	T=0.0169	C=0.9831
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.003	C=0.997
A Vietnamese Genetic Variation Database	Global	Study-wide	614	T=0.008	C=0.992
Northern Sweden	ACPOP	Study-wide	600	T=0.002	C=0.998
SGDP_PRJ	Global	Study-wide	552	T=0.045	C=0.955
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.066	C=0.934
FINRISK	Finnish from FINRISK project	Study-wide	304	T=0.003	C=0.997
Qatari	Global	Study-wide	216	T=0.106	C=0.894
HapMap	Global	Study-wide	198	T=0.025	C=0.975
HapMap	American	Sub	108	T=0.009	C=0.991
HapMap	Asian	Sub	90	T=0.04	C=0.96
Siberian	Global	Study-wide	56	T=0.00	C=1.00
The Danish reference pan genome	Danish	Study-wide	40	T=0.00	C=1.00

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 20	NC_000020.11:g.18525972T>C
GRCh37.p13 chr 20	NC_000020.10:g.18506616T>C
SEC23B RefSeqGene (LRG_1134)	NG_016281.2:g.23491T>C

Gene: SEC23B, SEC23 homolog B, COPII coat complex component (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SEC23B transcript variant 4	NM_001172745.3:c.834+40T>C	N/A	Intron Variant
SEC23B transcript variant 5	NM_001172746.3:c.780+40T>C	N/A	Intron Variant
SEC23B transcript variant 1	NM_006363.6:c.834+40T>C	N/A	Intron Variant
SEC23B transcript variant 2	NM_032985.6:c.834+40T>C	N/A	Intron Variant
SEC23B transcript variant 3	NM_032986.5:c.834+40T>C	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.

Allele: C (allele ID: 1257064 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001670710.2	not provided	Benign
RCV001807499.2	Congenital dyserythropoietic anemia, type II	Benign
RCV001807500.2	Cowden syndrome 7	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	T=	C
GRCh38.p14 chr 20	NC_000020.11:g.18525972=	NC_000020.11:g.18525972T>C
GRCh37.p13 chr 20	NC_000020.10:g.18506616=	NC_000020.10:g.18506616T>C
SEC23B RefSeqGene (LRG_1134)	NG_016281.2:g.23491=	NG_016281.2:g.23491T>C
SEC23B transcript variant 4	NM_001172745.1:c.834+40=	NM_001172745.1:c.834+40T>C
SEC23B transcript variant 4	NM_001172745.3:c.834+40=	NM_001172745.3:c.834+40T>C
SEC23B transcript variant 5	NM_001172746.1:c.780+40=	NM_001172746.1:c.780+40T>C
SEC23B transcript variant 5	NM_001172746.3:c.780+40=	NM_001172746.3:c.780+40T>C
SEC23B transcript variant 1	NM_006363.4:c.834+40=	NM_006363.4:c.834+40T>C
SEC23B transcript variant 1	NM_006363.6:c.834+40=	NM_006363.6:c.834+40T>C
SEC23B transcript variant 2	NM_032985.4:c.834+40=	NM_032985.4:c.834+40T>C
SEC23B transcript variant 2	NM_032985.6:c.834+40=	NM_032985.6:c.834+40T>C
SEC23B transcript variant 3	NM_032986.3:c.834+40=	NM_032986.3:c.834+40T>C
SEC23B transcript variant 3	NM_032986.5:c.834+40=	NM_032986.5:c.834+40T>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#.

102 SubSNP, 25 Frequency, 3 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1345335	Oct 05, 2000 (86)
2	TSC-CSHL	ss5168895	Oct 08, 2002 (108)
3	SC_JCM	ss5898484	Feb 20, 2003 (111)
4	SC_SNP	ss8342107	Apr 21, 2003 (114)
5	WI_SSAHASNP	ss12497767	Jul 11, 2003 (116)
6	CSHL-HAPMAP	ss16903510	Feb 27, 2004 (120)
7	CSHL-HAPMAP	ss17701612	Feb 27, 2004 (120)
8	SSAHASNP	ss21789608	Apr 05, 2004 (121)
9	PERLEGEN	ss23645262	Sep 20, 2004 (123)
10	HGSV	ss77481153	Dec 07, 2007 (129)
11	BCMHGSC_JDW	ss91658788	Mar 24, 2008 (129)
12	HUMANGENOME_JCVI	ss96189035	Feb 06, 2009 (130)
13	BGI	ss106181982	Feb 06, 2009 (130)
14	1000GENOMES	ss111824648	Jan 25, 2009 (130)
15	1000GENOMES	ss113168268	Jan 25, 2009 (130)
16	ENSEMBL	ss135750675	Dec 01, 2009 (131)
17	ENSEMBL	ss138220057	Dec 01, 2009 (131)
18	GMI	ss156240447	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss169261783	Jul 04, 2010 (132)
20	BUSHMAN	ss203850090	Jul 04, 2010 (132)
21	BCM-HGSC-SUB	ss208598105	Jul 04, 2010 (132)
22	1000GENOMES	ss228290482	Jul 14, 2010 (132)
23	1000GENOMES	ss237789196	Jul 15, 2010 (132)
24	1000GENOMES	ss243969562	Jul 15, 2010 (132)
25	BL	ss255524317	May 09, 2011 (134)
26	GMI	ss283324454	May 04, 2012 (137)
27	GMI	ss287434008	Apr 25, 2013 (138)
28	PJP	ss292625056	May 09, 2011 (134)
29	1000GENOMES	ss491173433	May 04, 2012 (137)
30	CLINSEQ_SNP	ss491806675	May 04, 2012 (137)
31	ILLUMINA	ss536471048	Sep 08, 2015 (146)
32	TISHKOFF	ss566174791	Apr 25, 2013 (138)
33	SSMP	ss662049614	Apr 25, 2013 (138)
34	NHLBI-ESP	ss713559551	Apr 25, 2013 (138)
35	EVA-GONL	ss994604591	Aug 21, 2014 (142)
36	JMKIDD_LAB	ss1067596616	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1082122252	Aug 21, 2014 (142)
38	1000GENOMES	ss1364299621	Aug 21, 2014 (142)
39	DDI	ss1429016085	Apr 01, 2015 (144)
40	EVA_GENOME_DK	ss1579464213	Apr 01, 2015 (144)
41	EVA_FINRISK	ss1584121976	Apr 01, 2015 (144)
42	EVA_UK10K_ALSPAC	ss1638541043	Apr 01, 2015 (144)
43	EVA_UK10K_TWINSUK	ss1681535076	Apr 01, 2015 (144)
44	EVA_EXAC	ss1693919322	Apr 01, 2015 (144)
45	EVA_DECODE	ss1698662550	Apr 01, 2015 (144)
46	EVA_MGP	ss1711534965	Apr 01, 2015 (144)
47	HAMMER_LAB	ss1809449432	Sep 08, 2015 (146)
48	WEILL_CORNELL_DGM	ss1938112186	Feb 12, 2016 (147)
49	GENOMED	ss1969107419	Jul 19, 2016 (147)
50	JJLAB	ss2029840406	Sep 14, 2016 (149)
51	USC_VALOUEV	ss2158393476	Dec 20, 2016 (150)
52	HUMAN_LONGEVITY	ss2241815387	Dec 20, 2016 (150)
53	SYSTEMSBIOZJU	ss2629415976	Nov 08, 2017 (151)
54	GRF	ss2704068206	Nov 08, 2017 (151)
55	GNOMAD	ss2744487637	Nov 08, 2017 (151)
56	GNOMAD	ss2750345997	Nov 08, 2017 (151)
57	GNOMAD	ss2966088241	Nov 08, 2017 (151)
58	SWEGEN	ss3017963685	Nov 08, 2017 (151)
59	BIOINF_KMB_FNS_UNIBA	ss3028753882	Nov 08, 2017 (151)
60	CSHL	ss3352449312	Nov 08, 2017 (151)
61	ILLUMINA	ss3628365726	Oct 12, 2018 (152)
62	OMUKHERJEE_ADBS	ss3646546787	Oct 12, 2018 (152)
63	URBANLAB	ss3650985287	Oct 12, 2018 (152)
64	EGCUT_WGS	ss3684685983	Jul 13, 2019 (153)
65	EVA_DECODE	ss3706677333	Jul 13, 2019 (153)
66	ACPOP	ss3743303014	Jul 13, 2019 (153)
67	EVA	ss3758498259	Jul 13, 2019 (153)
68	PACBIO	ss3788615955	Jul 13, 2019 (153)
69	PACBIO	ss3793513909	Jul 13, 2019 (153)
70	PACBIO	ss3798401086	Jul 13, 2019 (153)
71	KHV_HUMAN_GENOMES	ss3821668540	Jul 13, 2019 (153)
72	EVA	ss3825354490	Apr 27, 2020 (154)
73	EVA	ss3825949397	Apr 27, 2020 (154)
74	EVA	ss3835620457	Apr 27, 2020 (154)
75	EVA	ss3846944452	Apr 27, 2020 (154)
76	SGDP_PRJ	ss3888856136	Apr 27, 2020 (154)
77	KRGDB	ss3939056673	Apr 27, 2020 (154)
78	KOGIC	ss3981931388	Apr 27, 2020 (154)
79	FSA-LAB	ss3984213308	Apr 27, 2021 (155)
80	EVA	ss3986824550	Apr 27, 2021 (155)
81	TOPMED	ss5084315911	Apr 27, 2021 (155)
82	TOMMO_GENOMICS	ss5229102694	Apr 27, 2021 (155)
83	EVA	ss5237251119	Apr 27, 2021 (155)
84	1000G_HIGH_COVERAGE	ss5308289236	Oct 16, 2022 (156)
85	EVA	ss5436639145	Oct 16, 2022 (156)
86	HUGCELL_USP	ss5500672539	Oct 16, 2022 (156)
87	EVA	ss5512176365	Oct 16, 2022 (156)
88	1000G_HIGH_COVERAGE	ss5614475466	Oct 16, 2022 (156)
89	EVA	ss5623980554	Oct 16, 2022 (156)
90	EVA	ss5624112159	Oct 16, 2022 (156)
91	SANFORD_IMAGENETICS	ss5662983008	Oct 16, 2022 (156)
92	TOMMO_GENOMICS	ss5788162952	Oct 16, 2022 (156)
93	EVA	ss5800074274	Oct 16, 2022 (156)
94	EVA	ss5800228533	Oct 16, 2022 (156)
95	YY_MCH	ss5817869161	Oct 16, 2022 (156)
96	EVA	ss5845528362	Oct 16, 2022 (156)
97	EVA	ss5848544667	Oct 16, 2022 (156)
98	EVA	ss5853095603	Oct 16, 2022 (156)
99	EVA	ss5922912837	Oct 16, 2022 (156)
100	EVA	ss5957893856	Oct 16, 2022 (156)
101	EVA	ss5981079851	Oct 16, 2022 (156)
102	EVA	ss5981316446	Oct 16, 2022 (156)
103	1000Genomes	NC_000020.10 - 18506616	Oct 12, 2018 (152)
104	1000Genomes_30x	NC_000020.11 - 18525972	Oct 16, 2022 (156)
105	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 18506616	Oct 12, 2018 (152)
106	Genetic variation in the Estonian population	NC_000020.10 - 18506616	Oct 12, 2018 (152)
107	ExAC	NC_000020.10 - 18506616	Oct 12, 2018 (152)
108	FINRISK	NC_000020.10 - 18506616	Apr 27, 2020 (154)
109	The Danish reference pan genome	NC_000020.10 - 18506616	Apr 27, 2020 (154)
110	gnomAD - Genomes	NC_000020.11 - 18525972	Apr 27, 2021 (155)
111	gnomAD - Exomes	NC_000020.10 - 18506616	Jul 13, 2019 (153)
112	GO Exome Sequencing Project	NC_000020.10 - 18506616	Oct 12, 2018 (152)
113	Genome of the Netherlands Release 5	NC_000020.10 - 18506616	Apr 27, 2020 (154)
114	HapMap	NC_000020.11 - 18525972	Apr 27, 2020 (154)
115	KOREAN population from KRGDB	NC_000020.10 - 18506616	Apr 27, 2020 (154)
116	Korean Genome Project	NC_000020.11 - 18525972	Apr 27, 2020 (154)
117	Medical Genome Project healthy controls from Spanish population	NC_000020.10 - 18506616	Apr 27, 2020 (154)
118	Northern Sweden	NC_000020.10 - 18506616	Jul 13, 2019 (153)
119	Qatari	NC_000020.10 - 18506616	Apr 27, 2020 (154)
120	SGDP_PRJ	NC_000020.10 - 18506616	Apr 27, 2020 (154)
121	Siberian	NC_000020.10 - 18506616	Apr 27, 2020 (154)
122	8.3KJPN	NC_000020.10 - 18506616	Apr 27, 2021 (155)
123	14KJPN	NC_000020.11 - 18525972	Oct 16, 2022 (156)
124	TopMed	NC_000020.11 - 18525972	Apr 27, 2021 (155)
125	UK 10K study - Twins	NC_000020.10 - 18506616	Oct 12, 2018 (152)
126	A Vietnamese Genetic Variation Database	NC_000020.10 - 18506616	Jul 13, 2019 (153)
127	ALFA	NC_000020.11 - 18525972	Apr 27, 2021 (155)
128	ClinVar	RCV001670710.2	Oct 16, 2022 (156)
129	ClinVar	RCV001807499.2	Oct 16, 2022 (156)
130	ClinVar	RCV001807500.2	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77481153, ss91658788, ss111824648, ss113168268, ss169261783, ss203850090, ss208598105, ss255524317, ss283324454, ss287434008, ss292625056, ss491806675, ss1698662550	NC_000020.9:18454615:T:C	NC_000020.11:18525971:T:C	(self)
77747479, 43046076, 30424231, 5468431, 118437, 5629152, 13806717, 1811403, 19181527, 46234067, 650725, 16587879, 20154108, 40873116, 10909830, 87072001, 43046076, 9505339, ss228290482, ss237789196, ss243969562, ss491173433, ss536471048, ss566174791, ss662049614, ss713559551, ss994604591, ss1067596616, ss1082122252, ss1364299621, ss1429016085, ss1579464213, ss1584121976, ss1638541043, ss1681535076, ss1693919322, ss1711534965, ss1809449432, ss1938112186, ss1969107419, ss2029840406, ss2158393476, ss2629415976, ss2704068206, ss2744487637, ss2750345997, ss2966088241, ss3017963685, ss3352449312, ss3628365726, ss3646546787, ss3684685983, ss3743303014, ss3758498259, ss3788615955, ss3793513909, ss3798401086, ss3825354490, ss3825949397, ss3835620457, ss3888856136, ss3939056673, ss3984213308, ss3986824550, ss5229102694, ss5436639145, ss5512176365, ss5623980554, ss5624112159, ss5662983008, ss5800074274, ss5800228533, ss5845528362, ss5848544667, ss5957893856, ss5981079851, ss5981316446	NC_000020.10:18506615:T:C	NC_000020.11:18525971:T:C	(self)
RCV001670710.2, RCV001807499.2, RCV001807500.2, 102001401, 548155888, 2089689, 38309389, 122000056, 359424856, 9030914559, ss2241815387, ss3028753882, ss3650985287, ss3706677333, ss3821668540, ss3846944452, ss3981931388, ss5084315911, ss5237251119, ss5308289236, ss5500672539, ss5614475466, ss5788162952, ss5817869161, ss5853095603, ss5922912837	NC_000020.11:18525971:T:C	NC_000020.11:18525971:T:C	(self)
ss1345335, ss5168895, ss5898484, ss8342107, ss12497767, ss16903510, ss17701612, ss21789608, ss23645262, ss96189035, ss106181982, ss135750675, ss138220057, ss156240447	NT_011387.8:18446615:T:C	NC_000020.11:18525971: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 rs911115

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs911115