Name: rs11466155
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.

rs11466155

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:49510638 (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: T=0.235528 (62342/264690, TOPMED)
T=0.306952 (76854/250378, GnomAD_exome)
T=0.250250 (34989/139816, GnomAD) (+ 20 more)
T=0.305999 (37084/121190, ExAC)
T=0.305801 (33517/109604, ALFA)
T=0.05556 (1570/28258, 14KJPN)
T=0.05501 (922/16760, 8.3KJPN)
T=0.24958 (3246/13006, GO-ESP)
T=0.2275 (1457/6404, 1000G_30x)
T=0.2298 (1151/5008, 1000G)
T=0.3688 (1652/4480, Estonian)
T=0.3329 (1283/3854, ALSPAC)
T=0.3417 (1267/3708, TWINSUK)
T=0.0663 (194/2928, KOREAN)
T=0.342 (341/998, GoNL)
T=0.109 (67/613, Vietnamese)
T=0.360 (216/600, NorthernSweden)
T=0.277 (148/534, MGP)
T=0.334 (101/302, FINRISK)
C=0.389 (91/234, SGDP_PRJ)
T=0.162 (35/216, Qatari)
T=0.30 (12/40, GENOME_DK)
C=0.44 (14/32, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NGFR : Synonymous Variant
NGFR-AS1 : Intron Variant
MIR6165 : 2KB Upstream Variant
Publications: 2 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	125928	C=0.701115	T=0.298885
European	Sub	93594	C=0.66998	T=0.33002
African	Sub	13228	C=0.91344	T=0.08656
African Others	Sub	466	C=0.974	T=0.026
African American	Sub	12762	C=0.91122	T=0.08878
Asian	Sub	552	C=0.926	T=0.074
East Asian	Sub	454	C=0.936	T=0.064
Other Asian	Sub	98	C=0.88	T=0.12
Latin American 1	Sub	940	C=0.765	T=0.235
Latin American 2	Sub	4976	C=0.6746	T=0.3254
South Asian	Sub	178	C=0.618	T=0.382
Other	Sub	12460	C=0.70658	T=0.29342

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=0.764472	T=0.235528
gnomAD - Exomes	Global	Study-wide	250378	C=0.693048	T=0.306952
gnomAD - Exomes	European	Sub	134402	C=0.664715	T=0.335285
gnomAD - Exomes	Asian	Sub	48992	C=0.68677	T=0.31323
gnomAD - Exomes	American	Sub	34560	C=0.67740	T=0.32260
gnomAD - Exomes	African	Sub	16234	C=0.92393	T=0.07607
gnomAD - Exomes	Ashkenazi Jewish	Sub	10060	C=0.77773	T=0.22227
gnomAD - Exomes	Other	Sub	6130	C=0.7023	T=0.2977
gnomAD - Genomes	Global	Study-wide	139816	C=0.749750	T=0.250250
gnomAD - Genomes	European	Sub	75700	C=0.65618	T=0.34382
gnomAD - Genomes	African	Sub	41908	C=0.91856	T=0.08144
gnomAD - Genomes	American	Sub	13622	C=0.71113	T=0.28887
gnomAD - Genomes	Ashkenazi Jewish	Sub	3316	C=0.7711	T=0.2289
gnomAD - Genomes	East Asian	Sub	3120	C=0.9035	T=0.0965
gnomAD - Genomes	Other	Sub	2150	C=0.7423	T=0.2577
ExAC	Global	Study-wide	121190	C=0.694001	T=0.305999
ExAC	Europe	Sub	73264	C=0.67283	T=0.32717
ExAC	Asian	Sub	25132	C=0.67412	T=0.32588
ExAC	American	Sub	11562	C=0.66753	T=0.33247
ExAC	African	Sub	10330	C=0.92139	T=0.07861
ExAC	Other	Sub	902	C=0.703	T=0.297
Allele Frequency Aggregator	Total	Global	109604	C=0.694199	T=0.305801
Allele Frequency Aggregator	European	Sub	83530	C=0.66995	T=0.33005
Allele Frequency Aggregator	Other	Sub	11036	C=0.70497	T=0.29503
Allele Frequency Aggregator	African	Sub	8392	C=0.9115	T=0.0885
Allele Frequency Aggregator	Latin American 2	Sub	4976	C=0.6746	T=0.3254
Allele Frequency Aggregator	Latin American 1	Sub	940	C=0.765	T=0.235
Allele Frequency Aggregator	Asian	Sub	552	C=0.926	T=0.074
Allele Frequency Aggregator	South Asian	Sub	178	C=0.618	T=0.382
14KJPN	JAPANESE	Study-wide	28258	C=0.94444	T=0.05556
8.3KJPN	JAPANESE	Study-wide	16760	C=0.94499	T=0.05501
GO Exome Sequencing Project	Global	Study-wide	13006	C=0.75042	T=0.24958
GO Exome Sequencing Project	European American	Sub	8600	C=0.6688	T=0.3312
GO Exome Sequencing Project	African American	Sub	4406	C=0.9097	T=0.0903
1000Genomes_30x	Global	Study-wide	6404	C=0.7725	T=0.2275
1000Genomes_30x	African	Sub	1786	C=0.9530	T=0.0470
1000Genomes_30x	Europe	Sub	1266	C=0.6801	T=0.3199
1000Genomes_30x	South Asian	Sub	1202	C=0.5308	T=0.4692
1000Genomes_30x	East Asian	Sub	1170	C=0.9205	T=0.0795
1000Genomes_30x	American	Sub	980	C=0.683	T=0.317
1000Genomes	Global	Study-wide	5008	C=0.7702	T=0.2298
1000Genomes	African	Sub	1322	C=0.9523	T=0.0477
1000Genomes	East Asian	Sub	1008	C=0.9177	T=0.0823
1000Genomes	Europe	Sub	1006	C=0.6769	T=0.3231
1000Genomes	South Asian	Sub	978	C=0.528	T=0.472
1000Genomes	American	Sub	694	C=0.686	T=0.314
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.6312	T=0.3688
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.6671	T=0.3329
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.6583	T=0.3417
KOREAN population from KRGDB	KOREAN	Study-wide	2928	C=0.9337	T=0.0663
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.658	T=0.342
A Vietnamese Genetic Variation Database	Global	Study-wide	613	C=0.891	T=0.109
Northern Sweden	ACPOP	Study-wide	600	C=0.640	T=0.360
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	C=0.723	T=0.277
FINRISK	Finnish from FINRISK project	Study-wide	302	C=0.666	T=0.334
SGDP_PRJ	Global	Study-wide	234	C=0.389	T=0.611
Qatari	Global	Study-wide	216	C=0.838	T=0.162
The Danish reference pan genome	Danish	Study-wide	40	C=0.70	T=0.30
Siberian	Global	Study-wide	32	C=0.44	T=0.56

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 17	NC_000017.11:g.49510638C>T
GRCh37.p13 chr 17	NC_000017.10:g.47588000C>T

Gene: NGFR, nerve growth factor receptor (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NGFR transcript	NM_002507.4:c.795C>T	G [GGC] > G [GGT]	Coding Sequence Variant
tumor necrosis factor receptor superfamily member 16 precursor	NP_002498.1:p.Gly265=	G (Gly) > G (Gly)	Synonymous Variant

Gene: NGFR-AS1, NGFR antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NGFR-AS1 transcript	NR_103773.1:n.	N/A	Intron Variant

Gene: MIR6165, microRNA 6165 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
MIR6165 transcript	NR_106751.1: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.

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 17	NC_000017.11:g.49510638=	NC_000017.11:g.49510638C>T
GRCh37.p13 chr 17	NC_000017.10:g.47588000=	NC_000017.10:g.47588000C>T
NGFR transcript	NM_002507.4:c.795=	NM_002507.4:c.795C>T
NGFR transcript	NM_002507.3:c.795=	NM_002507.3:c.795C>T
tumor necrosis factor receptor superfamily member 16 precursor	NP_002498.1:p.Gly265=	NP_002498.1:p.Gly265=

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#.

106 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	IIPGA-WEISS-MARTINEZ	ss15356316	Feb 28, 2004 (120)
2	MGC_GENOME_DIFF	ss28498839	Sep 24, 2004 (126)
3	MGC_GENOME_DIFF	ss28513806	Sep 24, 2004 (126)
4	WIPGA	ss35528711	May 24, 2005 (125)
5	APPLERA_GI	ss48425547	Mar 10, 2006 (126)
6	HGSV	ss82643120	Dec 14, 2007 (130)
7	BCMHGSC_JDW	ss90607015	Mar 24, 2008 (129)
8	1000GENOMES	ss109792732	Jan 24, 2009 (130)
9	SEATTLESEQ	ss159735781	Dec 01, 2009 (131)
10	ILLUMINA	ss159978148	Dec 01, 2009 (131)
11	COMPLETE_GENOMICS	ss171495241	Jul 04, 2010 (132)
12	1000GENOMES	ss217326251	Jul 14, 2010 (132)
13	1000GENOMES	ss217405424	Jul 14, 2010 (132)
14	1000GENOMES	ss217407243	Jul 14, 2010 (132)
15	1000GENOMES	ss217414193	Jul 14, 2010 (132)
16	1000GENOMES	ss217425612	Jul 14, 2010 (132)
17	1000GENOMES	ss217430371	Jul 14, 2010 (132)
18	1000GENOMES	ss217432087	Jul 14, 2010 (132)
19	1000GENOMES	ss237259329	Jul 15, 2010 (132)
20	1000GENOMES	ss243551954	Jul 15, 2010 (132)
21	BL	ss255666730	May 09, 2011 (134)
22	GMI	ss282780768	May 04, 2012 (137)
23	PJP	ss292060382	May 09, 2011 (134)
24	NHLBI-ESP	ss342457899	May 09, 2011 (134)
25	ILLUMINA	ss479978398	Sep 08, 2015 (146)
26	ILLUMINA	ss483633783	May 04, 2012 (137)
27	ILLUMINA	ss484169185	May 04, 2012 (137)
28	1000GENOMES	ss491126483	May 04, 2012 (137)
29	CLINSEQ_SNP	ss491739086	May 04, 2012 (137)
30	ILLUMINA	ss536358115	Sep 08, 2015 (146)
31	TISHKOFF	ss565297274	Apr 25, 2013 (138)
32	SSMP	ss661105079	Apr 25, 2013 (138)
33	ILLUMINA	ss780552736	Sep 08, 2015 (146)
34	ILLUMINA	ss782530467	Sep 08, 2015 (146)
35	ILLUMINA	ss836044835	Sep 08, 2015 (146)
36	EVA-GONL	ss993153133	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1067572710	Aug 21, 2014 (142)
38	JMKIDD_LAB	ss1081087228	Aug 21, 2014 (142)
39	1000GENOMES	ss1358830230	Aug 21, 2014 (142)
40	DDI	ss1428044771	Apr 01, 2015 (144)
41	EVA_GENOME_DK	ss1578175386	Apr 01, 2015 (144)
42	EVA_FINRISK	ss1584107122	Apr 01, 2015 (144)
43	EVA_UK10K_ALSPAC	ss1635736164	Apr 01, 2015 (144)
44	EVA_UK10K_TWINSUK	ss1678730197	Apr 01, 2015 (144)
45	EVA_EXAC	ss1692847681	Apr 01, 2015 (144)
46	EVA_DECODE	ss1697196121	Apr 01, 2015 (144)
47	EVA_MGP	ss1711464982	Apr 01, 2015 (144)
48	WEILL_CORNELL_DGM	ss1936615403	Feb 12, 2016 (147)
49	GENOMED	ss1968398210	Jul 19, 2016 (147)
50	JJLAB	ss2029083723	Sep 14, 2016 (149)
51	USC_VALOUEV	ss2157559451	Dec 20, 2016 (150)
52	HUMAN_LONGEVITY	ss2217179953	Dec 20, 2016 (150)
53	SYSTEMSBIOZJU	ss2629037376	Nov 08, 2017 (151)
54	ILLUMINA	ss2633401734	Nov 08, 2017 (151)
55	GRF	ss2702119295	Nov 08, 2017 (151)
56	ILLUMINA	ss2710852694	Nov 08, 2017 (151)
57	GNOMAD	ss2742826875	Nov 08, 2017 (151)
58	GNOMAD	ss2749807543	Nov 08, 2017 (151)
59	GNOMAD	ss2950413499	Nov 08, 2017 (151)
60	SWEGEN	ss3015615326	Nov 08, 2017 (151)
61	EVA_SAMSUNG_MC	ss3023070793	Nov 08, 2017 (151)
62	BIOINF_KMB_FNS_UNIBA	ss3028363656	Nov 08, 2017 (151)
63	CSHL	ss3351764074	Nov 08, 2017 (151)
64	ILLUMINA	ss3627679947	Oct 12, 2018 (152)
65	ILLUMINA	ss3631382477	Oct 12, 2018 (152)
66	ILLUMINA	ss3636367381	Oct 12, 2018 (152)
67	ILLUMINA	ss3641994641	Oct 12, 2018 (152)
68	OMUKHERJEE_ADBS	ss3646513391	Oct 12, 2018 (152)
69	ILLUMINA	ss3652203224	Oct 12, 2018 (152)
70	EGCUT_WGS	ss3682488665	Jul 13, 2019 (153)
71	EVA_DECODE	ss3700559002	Jul 13, 2019 (153)
72	ACPOP	ss3742065568	Jul 13, 2019 (153)
73	EVA	ss3754720310	Jul 13, 2019 (153)
74	PACBIO	ss3788220336	Jul 13, 2019 (153)
75	PACBIO	ss3793174960	Jul 13, 2019 (153)
76	PACBIO	ss3798060721	Jul 13, 2019 (153)
77	KHV_HUMAN_GENOMES	ss3819987417	Jul 13, 2019 (153)
78	EVA	ss3825127789	Apr 27, 2020 (154)
79	EVA	ss3825531588	Apr 27, 2020 (154)
80	EVA	ss3825902131	Apr 27, 2020 (154)
81	EVA	ss3834891313	Apr 27, 2020 (154)
82	EVA	ss3841057657	Apr 27, 2020 (154)
83	EVA	ss3846554658	Apr 27, 2020 (154)
84	SGDP_PRJ	ss3885846519	Apr 27, 2020 (154)
85	KRGDB	ss3935559725	Apr 27, 2020 (154)
86	FSA-LAB	ss3984118284	Apr 27, 2021 (155)
87	EVA	ss3986732014	Apr 27, 2021 (155)
88	TOPMED	ss5037554835	Apr 27, 2021 (155)
89	TOMMO_GENOMICS	ss5222648914	Apr 27, 2021 (155)
90	EVA	ss5236944275	Apr 27, 2021 (155)
91	EVA	ss5237669309	Oct 16, 2022 (156)
92	1000G_HIGH_COVERAGE	ss5303296370	Oct 16, 2022 (156)
93	EVA	ss5427879119	Oct 16, 2022 (156)
94	HUGCELL_USP	ss5496326971	Oct 16, 2022 (156)
95	1000G_HIGH_COVERAGE	ss5607092196	Oct 16, 2022 (156)
96	EVA	ss5624073781	Oct 16, 2022 (156)
97	SANFORD_IMAGENETICS	ss5660192550	Oct 16, 2022 (156)
98	TOMMO_GENOMICS	ss5778934351	Oct 16, 2022 (156)
99	EVA	ss5799459167	Oct 16, 2022 (156)
100	EVA	ss5800209739	Oct 16, 2022 (156)
101	YY_MCH	ss5816580089	Oct 16, 2022 (156)
102	EVA	ss5834047976	Oct 16, 2022 (156)
103	EVA	ss5848452437	Oct 16, 2022 (156)
104	EVA	ss5851824287	Oct 16, 2022 (156)
105	EVA	ss5914108723	Oct 16, 2022 (156)
106	EVA	ss5951581117	Oct 16, 2022 (156)
107	1000Genomes	NC_000017.10 - 47588000	Oct 12, 2018 (152)
108	1000Genomes_30x	NC_000017.11 - 49510638	Oct 16, 2022 (156)
109	The Avon Longitudinal Study of Parents and Children	NC_000017.10 - 47588000	Oct 12, 2018 (152)
110	Genetic variation in the Estonian population	NC_000017.10 - 47588000	Oct 12, 2018 (152)
111	ExAC	NC_000017.10 - 47588000	Oct 12, 2018 (152)
112	FINRISK	NC_000017.10 - 47588000	Apr 27, 2020 (154)
113	The Danish reference pan genome	NC_000017.10 - 47588000	Apr 27, 2020 (154)
114	gnomAD - Genomes	NC_000017.11 - 49510638	Apr 27, 2021 (155)
115	gnomAD - Exomes	NC_000017.10 - 47588000	Jul 13, 2019 (153)
116	GO Exome Sequencing Project	NC_000017.10 - 47588000	Oct 12, 2018 (152)
117	Genome of the Netherlands Release 5	NC_000017.10 - 47588000	Apr 27, 2020 (154)
118	KOREAN population from KRGDB	NC_000017.10 - 47588000	Apr 27, 2020 (154)
119	Medical Genome Project healthy controls from Spanish population	NC_000017.10 - 47588000	Apr 27, 2020 (154)
120	Northern Sweden	NC_000017.10 - 47588000	Jul 13, 2019 (153)
121	Qatari	NC_000017.10 - 47588000	Apr 27, 2020 (154)
122	SGDP_PRJ	NC_000017.10 - 47588000	Apr 27, 2020 (154)
123	Siberian	NC_000017.10 - 47588000	Apr 27, 2020 (154)
124	8.3KJPN	NC_000017.10 - 47588000	Apr 27, 2021 (155)
125	14KJPN	NC_000017.11 - 49510638	Oct 16, 2022 (156)
126	TopMed	NC_000017.11 - 49510638	Apr 27, 2021 (155)
127	UK 10K study - Twins	NC_000017.10 - 47588000	Oct 12, 2018 (152)
128	A Vietnamese Genetic Variation Database	NC_000017.10 - 47588000	Jul 13, 2019 (153)
129	ALFA	NC_000017.11 - 49510638	Apr 27, 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)
rs17846454	Mar 10, 2006 (126)
rs17859504	Mar 10, 2006 (126)
rs57836330	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss82643120, ss90607015, ss109792732, ss171495241, ss217326251, ss217405424, ss217407243, ss217414193, ss217425612, ss217430371, ss217432087, ss255666730, ss282780768, ss292060382, ss483633783, ss491739086, ss1697196121	NC_000017.9:44942998:C:T	NC_000017.11:49510637:C:T	(self)
72078917, 39942584, 28226913, 3296299, 103583, 4376977, 12130802, 1584865, 17802277, 42737119, 580742, 15350433, 18657325, 37863499, 10075805, 80618221, 39942584, 8835711, ss237259329, ss243551954, ss342457899, ss479978398, ss484169185, ss491126483, ss536358115, ss565297274, ss661105079, ss780552736, ss782530467, ss836044835, ss993153133, ss1067572710, ss1081087228, ss1358830230, ss1428044771, ss1578175386, ss1584107122, ss1635736164, ss1678730197, ss1692847681, ss1711464982, ss1936615403, ss1968398210, ss2029083723, ss2157559451, ss2629037376, ss2633401734, ss2702119295, ss2710852694, ss2742826875, ss2749807543, ss2950413499, ss3015615326, ss3023070793, ss3351764074, ss3627679947, ss3631382477, ss3636367381, ss3641994641, ss3646513391, ss3652203224, ss3682488665, ss3742065568, ss3754720310, ss3788220336, ss3793174960, ss3798060721, ss3825127789, ss3825531588, ss3825902131, ss3834891313, ss3841057657, ss3885846519, ss3935559725, ss3984118284, ss3986732014, ss5222648914, ss5427879119, ss5624073781, ss5660192550, ss5799459167, ss5800209739, ss5834047976, ss5848452437, ss5951581117	NC_000017.10:47587999:C:T	NC_000017.11:49510637:C:T	(self)
94618131, 508617842, 112771455, 253100497, 3854306861, ss2217179953, ss3028363656, ss3700559002, ss3819987417, ss3846554658, ss5037554835, ss5236944275, ss5237669309, ss5303296370, ss5496326971, ss5607092196, ss5778934351, ss5816580089, ss5851824287, ss5914108723	NC_000017.11:49510637:C:T	NC_000017.11:49510637:C:T	(self)
ss15356316, ss28498839, ss28513806, ss35528711, ss48425547, ss159735781, ss159978148	NT_010783.15:12862151:C:T	NC_000017.11:49510637:C:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

2 citations for rs11466155

PMID	Title	Author	Year	Journal
21791469	Genetic factors underlying the risk of bortezomib induced peripheral neuropathy in multiple myeloma patients.	Corthals SL et al.	2011	Haematologica
29028593	Genetic variations in the p11/tPA/BDNF pathway are associated with post stroke depression.	Liang J et al.	2018	Journal of affective disorders

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs11466155