rs796052641

Orientation

minus

Stabilized

minus

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

Make rs796052641(C;T)

Make rs796052641(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63438644

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052641
dbSNP (classic)	rs796052641
ClinGen	rs796052641
ebi	rs796052641
HLI	rs796052641
Exac	rs796052641
Gnomad	rs796052641
Varsome	rs796052641
LitVar	rs796052641
Map	rs796052641
PheGenI	rs796052641
Biobank	rs796052641
1000 genomes	rs796052641
hgdp	rs796052641
ensembl	rs796052641
geneview	rs796052641
scholar	rs796052641
google	rs796052641
pharmgkb	rs796052641
gwascentral	rs796052641
openSNP	rs796052641
23andMe	rs796052641
SNPshot	rs796052641
SNPdbe	rs796052641
MSV3d	rs796052641
GWAS Ctlg	rs796052641

Max Magnitude

0

ClinVar
Risk	rs796052641(T;T)
Alt	rs796052641(T;T)
Reference	Rs796052641(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62069997G>A
CLNSRC
CLNACC	RCV000187889.1,