rs796052625

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs796052625(C;C)

Make rs796052625(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63444737

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052625
dbSNP (classic)	rs796052625
ClinGen	rs796052625
ebi	rs796052625
HLI	rs796052625
Exac	rs796052625
Gnomad	rs796052625
Varsome	rs796052625
LitVar	rs796052625
Map	rs796052625
PheGenI	rs796052625
Biobank	rs796052625
1000 genomes	rs796052625
hgdp	rs796052625
ensembl	rs796052625
geneview	rs796052625
scholar	rs796052625
google	rs796052625
pharmgkb	rs796052625
gwascentral	rs796052625
openSNP	rs796052625
23andMe	rs796052625
SNPshot	rs796052625
SNPdbe	rs796052625
MSV3d	rs796052625
GWAS Ctlg	rs796052625

Max Magnitude

0

ClinVar
Risk	rs796052625(C;C) rs796052625(T;T)
Alt	rs796052625(C;C) rs796052625(T;T)
Reference	Rs796052625(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62076090C>A; NC_000020.10:g.62076090C>G
CLNSRC
CLNACC	RCV000187861.2, RCV000187860.2,