rs796052642

Orientation

minus

Stabilized

minus

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

Make rs796052642(A;A)

Make rs796052642(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63438639

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052642
dbSNP (classic)	rs796052642
ClinGen	rs796052642
ebi	rs796052642
HLI	rs796052642
Exac	rs796052642
Gnomad	rs796052642
Varsome	rs796052642
LitVar	rs796052642
Map	rs796052642
PheGenI	rs796052642
Biobank	rs796052642
1000 genomes	rs796052642
hgdp	rs796052642
ensembl	rs796052642
geneview	rs796052642
scholar	rs796052642
google	rs796052642
pharmgkb	rs796052642
gwascentral	rs796052642
openSNP	rs796052642
23andMe	rs796052642
SNPshot	rs796052642
SNPdbe	rs796052642
MSV3d	rs796052642
GWAS Ctlg	rs796052642

Max Magnitude

0

ClinVar
Risk	rs796052642(A;A)
Alt	rs796052642(A;A)
Reference	Rs796052642(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62069992C>T
CLNSRC
CLNACC	RCV000187890.2,