rs796052644

Orientation

minus

Stabilized

minus

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

Make rs796052644(A;A)

Make rs796052644(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63433848

Gene	KCNQ2, LOC105372721

is a	snp
is	mentioned by
dbSNP	rs796052644
dbSNP (classic)	rs796052644
ClinGen	rs796052644
ebi	rs796052644
HLI	rs796052644
Exac	rs796052644
Gnomad	rs796052644
Varsome	rs796052644
LitVar	rs796052644
Map	rs796052644
PheGenI	rs796052644
Biobank	rs796052644
1000 genomes	rs796052644
hgdp	rs796052644
ensembl	rs796052644
geneview	rs796052644
scholar	rs796052644
google	rs796052644
pharmgkb	rs796052644
gwascentral	rs796052644
openSNP	rs796052644
23andMe	rs796052644
SNPshot	rs796052644
SNPdbe	rs796052644
MSV3d	rs796052644
GWAS Ctlg	rs796052644

Max Magnitude

0

ClinVar
Risk	rs796052644(A;A)
Alt	rs796052644(A;A)
Reference	Rs796052644(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62065201C>T
CLNSRC
CLNACC	RCV000187892.1,