rs796052614

Orientation

minus

Stabilized

minus

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

Make rs796052614(C;G)

Make rs796052614(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63472170

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052614
dbSNP (classic)	rs796052614
ClinGen	rs796052614
ebi	rs796052614
HLI	rs796052614
Exac	rs796052614
Gnomad	rs796052614
Varsome	rs796052614
LitVar	rs796052614
Map	rs796052614
PheGenI	rs796052614
Biobank	rs796052614
1000 genomes	rs796052614
hgdp	rs796052614
ensembl	rs796052614
geneview	rs796052614
scholar	rs796052614
google	rs796052614
pharmgkb	rs796052614
gwascentral	rs796052614
openSNP	rs796052614
23andMe	rs796052614
SNPshot	rs796052614
SNPdbe	rs796052614
MSV3d	rs796052614
GWAS Ctlg	rs796052614

Max Magnitude

0

ClinVar
Risk	rs796052614(G;G)
Alt	rs796052614(G;G)
Reference	Rs796052614(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62103523G>C
CLNSRC
CLNACC	RCV000187848.1,