Name: rs349358
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.

rs349358

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:72539240 (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>A / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.116604 (30864/264690, TOPMED)
C=0.121538 (17033/140146, GnomAD)
C=0.16425 (12483/75998, ALFA) (+ 19 more)
C=0.02459 (695/28258, 14KJPN)
C=0.02470 (414/16760, 8.3KJPN)
C=0.0962 (616/6404, 1000G_30x)
C=0.0962 (482/5008, 1000G)
C=0.2004 (898/4480, Estonian)
C=0.1837 (708/3854, ALSPAC)
C=0.1772 (657/3708, TWINSUK)
C=0.0440 (129/2930, KOREAN)
C=0.1305 (272/2084, HGDP_Stanford)
C=0.0798 (151/1892, HapMap)
C=0.0486 (89/1832, Korea1K)
C=0.183 (183/998, GoNL)
C=0.167 (100/600, NorthernSweden)
C=0.071 (39/550, SGDP_PRJ)
C=0.204 (44/216, Qatari)
C=0.047 (10/212, Vietnamese)
C=0.20 (11/54, Siberian)
C=0.08 (4/50, Ancient Sardinia)
C=0.17 (7/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KCNB2 : Intron Variant
Publications: 3 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	75998	C=0.16425	T=0.83575
European	Sub	59714	C=0.17664	T=0.82336
African	Sub	5204	C=0.0427	T=0.9573
African Others	Sub	182	C=0.005	T=0.995
African American	Sub	5022	C=0.0440	T=0.9560
Asian	Sub	238	C=0.025	T=0.975
East Asian	Sub	164	C=0.030	T=0.970
Other Asian	Sub	74	C=0.01	T=0.99
Latin American 1	Sub	400	C=0.147	T=0.853
Latin American 2	Sub	3390	C=0.0959	T=0.9041
South Asian	Sub	4966	C=0.2143	T=0.7857
Other	Sub	2086	C=0.1242	T=0.8758

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=0.116604	T=0.883396
gnomAD - Genomes	Global	Study-wide	140146	C=0.121538	T=0.878462
gnomAD - Genomes	European	Sub	75870	C=0.17102	T=0.82898
gnomAD - Genomes	African	Sub	42022	C=0.04084	T=0.95916
gnomAD - Genomes	American	Sub	13650	C=0.10586	T=0.89414
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.1477	T=0.8523
gnomAD - Genomes	East Asian	Sub	3132	C=0.0482	T=0.9518
gnomAD - Genomes	Other	Sub	2148	C=0.1187	T=0.8813
Allele Frequency Aggregator	Total	Global	75998	C=0.16425	T=0.83575
Allele Frequency Aggregator	European	Sub	59714	C=0.17664	T=0.82336
Allele Frequency Aggregator	African	Sub	5204	C=0.0427	T=0.9573
Allele Frequency Aggregator	South Asian	Sub	4966	C=0.2143	T=0.7857
Allele Frequency Aggregator	Latin American 2	Sub	3390	C=0.0959	T=0.9041
Allele Frequency Aggregator	Other	Sub	2086	C=0.1242	T=0.8758
Allele Frequency Aggregator	Latin American 1	Sub	400	C=0.147	T=0.853
Allele Frequency Aggregator	Asian	Sub	238	C=0.025	T=0.975
14KJPN	JAPANESE	Study-wide	28258	C=0.02459	T=0.97541
8.3KJPN	JAPANESE	Study-wide	16760	C=0.02470	T=0.97530
1000Genomes_30x	Global	Study-wide	6404	C=0.0962	T=0.9038
1000Genomes_30x	African	Sub	1786	C=0.0207	T=0.9793
1000Genomes_30x	Europe	Sub	1266	C=0.1738	T=0.8262
1000Genomes_30x	South Asian	Sub	1202	C=0.1938	T=0.8062
1000Genomes_30x	East Asian	Sub	1170	C=0.0308	T=0.9692
1000Genomes_30x	American	Sub	980	C=0.092	T=0.908
1000Genomes	Global	Study-wide	5008	C=0.0962	T=0.9038
1000Genomes	African	Sub	1322	C=0.0204	T=0.9796
1000Genomes	East Asian	Sub	1008	C=0.0298	T=0.9702
1000Genomes	Europe	Sub	1006	C=0.1690	T=0.8310
1000Genomes	South Asian	Sub	978	C=0.197	T=0.803
1000Genomes	American	Sub	694	C=0.089	T=0.911
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.2004	T=0.7996
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.1837	T=0.8163
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.1772	T=0.8228
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.0440	A=0.0000, T=0.9560
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.1305	T=0.8695
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.062	T=0.938
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.184	T=0.816
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.271	T=0.729
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.197	T=0.803
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.012	T=0.988
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.028	T=0.972
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.00	T=1.00
HapMap	Global	Study-wide	1892	C=0.0798	T=0.9202
HapMap	American	Sub	770	C=0.114	T=0.886
HapMap	African	Sub	692	C=0.027	T=0.973
HapMap	Asian	Sub	254	C=0.031	T=0.969
HapMap	Europe	Sub	176	C=0.205	T=0.795
Korean Genome Project	KOREAN	Study-wide	1832	C=0.0486	T=0.9514
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.183	T=0.817
Northern Sweden	ACPOP	Study-wide	600	C=0.167	T=0.833
SGDP_PRJ	Global	Study-wide	550	C=0.071	T=0.929
Qatari	Global	Study-wide	216	C=0.204	T=0.796
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.047	T=0.953
Siberian	Global	Study-wide	54	C=0.20	T=0.80
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	50	C=0.08	T=0.92
The Danish reference pan genome	Danish	Study-wide	40	C=0.17	T=0.82

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 8	NC_000008.11:g.72539240C>A
GRCh38.p14 chr 8	NC_000008.11:g.72539240C>T
GRCh37.p13 chr 8	NC_000008.10:g.73451475C>A
GRCh37.p13 chr 8	NC_000008.10:g.73451475C>T

Gene: KCNB2, potassium voltage-gated channel subfamily B member 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KCNB2 transcript	NM_004770.3:c.-94+1355C>A	N/A	Intron Variant
KCNB2 transcript variant X1	XM_017013982.2:c.	N/A	Genic 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=	A	T
GRCh38.p14 chr 8	NC_000008.11:g.72539240=	NC_000008.11:g.72539240C>A	NC_000008.11:g.72539240C>T
GRCh37.p13 chr 8	NC_000008.10:g.73451475=	NC_000008.10:g.73451475C>A	NC_000008.10:g.73451475C>T
KCNB2 transcript	NM_004770.2:c.-94+1355=	NM_004770.2:c.-94+1355C>A	NM_004770.2:c.-94+1355C>T
KCNB2 transcript	NM_004770.3:c.-94+1355=	NM_004770.3:c.-94+1355C>A	NM_004770.3:c.-94+1355C>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#.

110 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KWOK	ss444169	Jul 12, 2000 (79)
2	SC_JCM	ss611638	Jul 16, 2000 (80)
3	KWOK	ss1134155	Oct 05, 2000 (92)
4	KWOK	ss1928735	Oct 18, 2000 (92)
5	TSC-CSHL	ss3037276	Jun 15, 2001 (96)
6	SC_JCM	ss5902219	Feb 20, 2003 (111)
7	WI_SSAHASNP	ss11922322	Jul 11, 2003 (116)
8	WI_SSAHASNP	ss14342586	Dec 05, 2003 (119)
9	SSAHASNP	ss22685066	Apr 05, 2004 (121)
10	PERLEGEN	ss24503935	Sep 20, 2004 (123)
11	ABI	ss44870445	Mar 14, 2006 (126)
12	AFFY	ss66030793	Nov 30, 2006 (127)
13	AFFY	ss66361454	Nov 30, 2006 (127)
14	ILLUMINA	ss66778727	Nov 30, 2006 (127)
15	ILLUMINA	ss67295642	Nov 30, 2006 (127)
16	ILLUMINA	ss67699884	Nov 30, 2006 (127)
17	ILLUMINA	ss70774258	May 23, 2008 (130)
18	ILLUMINA	ss71350040	May 17, 2007 (127)
19	ILLUMINA	ss75782009	Dec 06, 2007 (129)
20	AFFY	ss76080464	Dec 06, 2007 (129)
21	HGSV	ss78945471	Dec 06, 2007 (129)
22	ILLUMINA	ss79161976	Dec 14, 2007 (130)
23	HGSV	ss83147488	Dec 14, 2007 (130)
24	KRIBB_YJKIM	ss83435387	Dec 14, 2007 (130)
25	BCMHGSC_JDW	ss93909165	Mar 25, 2008 (129)
26	HUMANGENOME_JCVI	ss98083193	Feb 03, 2009 (130)
27	BGI	ss105625012	Feb 03, 2009 (130)
28	1000GENOMES	ss108124002	Jan 23, 2009 (130)
29	1000GENOMES	ss113209875	Jan 25, 2009 (130)
30	ILLUMINA-UK	ss116009481	Feb 14, 2009 (130)
31	ILLUMINA	ss122191791	Dec 01, 2009 (131)
32	ENSEMBL	ss134338880	Dec 01, 2009 (131)
33	ENSEMBL	ss143559155	Dec 01, 2009 (131)
34	ILLUMINA	ss154260455	Dec 01, 2009 (131)
35	GMI	ss156507093	Dec 01, 2009 (131)
36	ILLUMINA	ss159437045	Dec 01, 2009 (131)
37	COMPLETE_GENOMICS	ss164975851	Jul 04, 2010 (132)
38	COMPLETE_GENOMICS	ss166760801	Jul 04, 2010 (132)
39	ILLUMINA	ss171589180	Jul 04, 2010 (132)
40	AFFY	ss172433269	Jul 04, 2010 (132)
41	ILLUMINA	ss173594898	Jul 04, 2010 (132)
42	BUSHMAN	ss199323272	Jul 04, 2010 (132)
43	BCM-HGSC-SUB	ss206470790	Jul 04, 2010 (132)
44	1000GENOMES	ss223776832	Jul 14, 2010 (132)
45	1000GENOMES	ss234487236	Jul 15, 2010 (132)
46	1000GENOMES	ss241333241	Jul 15, 2010 (132)
47	BL	ss254415914	May 09, 2011 (134)
48	GMI	ss279862203	May 04, 2012 (137)
49	GMI	ss285865452	Apr 25, 2013 (138)
50	PJP	ss294105462	May 09, 2011 (134)
51	ILLUMINA	ss537176762	Sep 08, 2015 (146)
52	TISHKOFF	ss560832810	Apr 25, 2013 (138)
53	SSMP	ss655268772	Apr 25, 2013 (138)
54	ILLUMINA	ss825492494	Apr 01, 2015 (144)
55	ILLUMINA	ss832948634	Jul 13, 2019 (153)
56	EVA-GONL	ss985658314	Aug 21, 2014 (142)
57	JMKIDD_LAB	ss1075625702	Aug 21, 2014 (142)
58	1000GENOMES	ss1330405650	Aug 21, 2014 (142)
59	DDI	ss1431555512	Apr 01, 2015 (144)
60	EVA_GENOME_DK	ss1582736576	Apr 01, 2015 (144)
61	EVA_DECODE	ss1595258351	Apr 01, 2015 (144)
62	EVA_UK10K_ALSPAC	ss1620929056	Apr 01, 2015 (144)
63	EVA_UK10K_TWINSUK	ss1663923089	Apr 01, 2015 (144)
64	EVA_SVP	ss1713045416	Apr 01, 2015 (144)
65	HAMMER_LAB	ss1805594021	Sep 08, 2015 (146)
66	WEILL_CORNELL_DGM	ss1928943593	Feb 12, 2016 (147)
67	GENOMED	ss1971009203	Jul 19, 2016 (147)
68	JJLAB	ss2025174000	Sep 14, 2016 (149)
69	USC_VALOUEV	ss2153399648	Dec 20, 2016 (150)
70	HUMAN_LONGEVITY	ss2304249620	Dec 20, 2016 (150)
71	SYSTEMSBIOZJU	ss2627065222	Nov 08, 2017 (151)
72	GRF	ss2709172771	Nov 08, 2017 (151)
73	GNOMAD	ss2868351294	Nov 08, 2017 (151)
74	SWEGEN	ss3003398770	Nov 08, 2017 (151)
75	BIOINF_KMB_FNS_UNIBA	ss3026373075	Nov 08, 2017 (151)
76	CSHL	ss3348241758	Nov 08, 2017 (151)
77	ILLUMINA	ss3630085967	Oct 12, 2018 (152)
78	ILLUMINA	ss3638767042	Oct 12, 2018 (152)
79	ILLUMINA	ss3639385920	Oct 12, 2018 (152)
80	ILLUMINA	ss3639722553	Oct 12, 2018 (152)
81	ILLUMINA	ss3643697463	Oct 12, 2018 (152)
82	URBANLAB	ss3648941795	Oct 12, 2018 (152)
83	EGCUT_WGS	ss3671088784	Jul 13, 2019 (153)
84	EVA_DECODE	ss3722279119	Jul 13, 2019 (153)
85	ACPOP	ss3735778878	Jul 13, 2019 (153)
86	EVA	ss3768164595	Jul 13, 2019 (153)
87	KHV_HUMAN_GENOMES	ss3811321605	Jul 13, 2019 (153)
88	EVA	ss3831229180	Apr 26, 2020 (154)
89	EVA	ss3839123781	Apr 26, 2020 (154)
90	EVA	ss3844583886	Apr 26, 2020 (154)
91	HGDP	ss3847917802	Apr 26, 2020 (154)
92	SGDP_PRJ	ss3870208510	Apr 26, 2020 (154)
93	KRGDB	ss3917741190	Apr 26, 2020 (154)
94	KOGIC	ss3964130803	Apr 26, 2020 (154)
95	EVA	ss3985367460	Apr 26, 2021 (155)
96	EVA	ss4017396643	Apr 26, 2021 (155)
97	TOPMED	ss4790954853	Apr 26, 2021 (155)
98	TOMMO_GENOMICS	ss5189316000	Apr 26, 2021 (155)
99	1000G_HIGH_COVERAGE	ss5277620357	Oct 14, 2022 (156)
100	EVA	ss5382035339	Oct 14, 2022 (156)
101	HUGCELL_USP	ss5474137648	Oct 14, 2022 (156)
102	EVA	ss5509404047	Oct 14, 2022 (156)
103	1000G_HIGH_COVERAGE	ss5568243764	Oct 14, 2022 (156)
104	SANFORD_IMAGENETICS	ss5645654353	Oct 14, 2022 (156)
105	TOMMO_GENOMICS	ss5731558514	Oct 14, 2022 (156)
106	YY_MCH	ss5809823817	Oct 14, 2022 (156)
107	EVA	ss5830719110	Oct 14, 2022 (156)
108	EVA	ss5856425612	Oct 14, 2022 (156)
109	EVA	ss5889515319	Oct 14, 2022 (156)
110	EVA	ss5974874392	Oct 14, 2022 (156)
111	1000Genomes	NC_000008.10 - 73451475	Oct 12, 2018 (152)
112	1000Genomes_30x	NC_000008.11 - 72539240	Oct 14, 2022 (156)
113	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 73451475	Oct 12, 2018 (152)
114	Genetic variation in the Estonian population	NC_000008.10 - 73451475	Oct 12, 2018 (152)
115	The Danish reference pan genome	NC_000008.10 - 73451475	Apr 26, 2020 (154)
116	gnomAD - Genomes	NC_000008.11 - 72539240	Apr 26, 2021 (155)
117	Genome of the Netherlands Release 5	NC_000008.10 - 73451475	Apr 26, 2020 (154)
118	HGDP-CEPH-db Supplement 1	NC_000008.9 - 73614029	Apr 26, 2020 (154)
119	HapMap	NC_000008.11 - 72539240	Apr 26, 2020 (154)
120	KOREAN population from KRGDB	NC_000008.10 - 73451475	Apr 26, 2020 (154)
121	Korean Genome Project	NC_000008.11 - 72539240	Apr 26, 2020 (154)
122	Northern Sweden	NC_000008.10 - 73451475	Jul 13, 2019 (153)
123	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000008.10 - 73451475	Apr 26, 2021 (155)
124	Qatari	NC_000008.10 - 73451475	Apr 26, 2020 (154)
125	SGDP_PRJ	NC_000008.10 - 73451475	Apr 26, 2020 (154)
126	Siberian	NC_000008.10 - 73451475	Apr 26, 2020 (154)
127	8.3KJPN	NC_000008.10 - 73451475	Apr 26, 2021 (155)
128	14KJPN	NC_000008.11 - 72539240	Oct 14, 2022 (156)
129	TopMed	NC_000008.11 - 72539240	Apr 26, 2021 (155)
130	UK 10K study - Twins	NC_000008.10 - 73451475	Oct 12, 2018 (152)
131	A Vietnamese Genetic Variation Database	NC_000008.10 - 73451475	Jul 13, 2019 (153)
132	ALFA	NC_000008.11 - 72539240	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)
rs829910	Jan 18, 2001 (92)
rs17828549	Oct 08, 2004 (123)
rs56753339	May 23, 2008 (130)
rs386583095	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
24918584, ss3917741190	NC_000008.10:73451474:C:A	NC_000008.11:72539239:C:A	(self)
595694, ss78945471, ss83147488, ss93909165, ss108124002, ss113209875, ss116009481, ss164975851, ss166760801, ss199323272, ss206470790, ss254415914, ss279862203, ss285865452, ss294105462, ss825492494, ss1595258351, ss1713045416, ss3639385920, ss3639722553, ss3643697463, ss3847917802	NC_000008.9:73614028:C:T	NC_000008.11:72539239:C:T	(self)
42548919, 23664881, 16827032, 8901514, 10563282, 24918584, 9063743, 593387, 10985523, 22225490, 5916002, 47285307, 23664881, 5263544, ss223776832, ss234487236, ss241333241, ss537176762, ss560832810, ss655268772, ss832948634, ss985658314, ss1075625702, ss1330405650, ss1431555512, ss1582736576, ss1620929056, ss1663923089, ss1805594021, ss1928943593, ss1971009203, ss2025174000, ss2153399648, ss2627065222, ss2709172771, ss2868351294, ss3003398770, ss3348241758, ss3630085967, ss3638767042, ss3671088784, ss3735778878, ss3768164595, ss3831229180, ss3839123781, ss3870208510, ss3917741190, ss3985367460, ss4017396643, ss5189316000, ss5382035339, ss5509404047, ss5645654353, ss5830719110, ss5974874392	NC_000008.10:73451474:C:T	NC_000008.11:72539239:C:T	(self)
55769699, 300035827, 3649021, 20508804, 65395618, 628332413, 14259348036, ss2304249620, ss3026373075, ss3648941795, ss3722279119, ss3811321605, ss3844583886, ss3964130803, ss4790954853, ss5277620357, ss5474137648, ss5568243764, ss5731558514, ss5809823817, ss5856425612, ss5889515319	NC_000008.11:72539239:C:T	NC_000008.11:72539239:C:T	(self)
ss11922322	NT_008183.16:25294023:C:T	NC_000008.11:72539239:C:T	(self)
ss14342586, ss22685066	NT_008183.17:25294023:C:T	NC_000008.11:72539239:C:T	(self)
ss444169, ss611638, ss1134155, ss1928735, ss3037276, ss5902219, ss24503935, ss44870445, ss66030793, ss66361454, ss66778727, ss67295642, ss67699884, ss70774258, ss71350040, ss75782009, ss76080464, ss79161976, ss83435387, ss98083193, ss105625012, ss122191791, ss134338880, ss143559155, ss154260455, ss156507093, ss159437045, ss171589180, ss172433269, ss173594898	NT_008183.19:25315875:C:T	NC_000008.11:72539239:C:T	(self)

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

3 citations for rs349358

PMID	Title	Author	Year	Journal
18676988	A high-density association screen of 155 ion transport genes for involvement with common migraine.	Nyholt DR et al.	2008	Human molecular genetics
31077873	Genetic contribution to PONV risk.	Klenke S et al.	2020	Anaesthesia, critical care & pain medicine
32371828	Genetic variability in postoperative nausea and vomiting: A systematic review.	Klenke S et al.	2020	European journal of anaesthesiology

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

rs349358