rs796052658

Orientation

minus

Stabilized

minus

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

Make rs796052658(G;T)

Make rs796052658(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63407018

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052658
dbSNP (classic)	rs796052658
ClinGen	rs796052658
ebi	rs796052658
HLI	rs796052658
Exac	rs796052658
Gnomad	rs796052658
Varsome	rs796052658
LitVar	rs796052658
Map	rs796052658
PheGenI	rs796052658
Biobank	rs796052658
1000 genomes	rs796052658
hgdp	rs796052658
ensembl	rs796052658
geneview	rs796052658
scholar	rs796052658
google	rs796052658
pharmgkb	rs796052658
gwascentral	rs796052658
openSNP	rs796052658
23andMe	rs796052658
SNPshot	rs796052658
SNPdbe	rs796052658
MSV3d	rs796052658
GWAS Ctlg	rs796052658

Max Magnitude

0

ClinVar
Risk	rs796052658(T;T)
Alt	rs796052658(T;T)
Reference	Rs796052658(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62038371C>A
CLNSRC
CLNACC	RCV000187933.2,