rs796052636

Orientation

minus

Stabilized

minus

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

Make rs796052636(A;A)

Make rs796052636(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63439681

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052636
dbSNP (classic)	rs796052636
ClinGen	rs796052636
ebi	rs796052636
HLI	rs796052636
Exac	rs796052636
Gnomad	rs796052636
Varsome	rs796052636
LitVar	rs796052636
Map	rs796052636
PheGenI	rs796052636
Biobank	rs796052636
1000 genomes	rs796052636
hgdp	rs796052636
ensembl	rs796052636
geneview	rs796052636
scholar	rs796052636
google	rs796052636
pharmgkb	rs796052636
gwascentral	rs796052636
openSNP	rs796052636
23andMe	rs796052636
SNPshot	rs796052636
SNPdbe	rs796052636
MSV3d	rs796052636
GWAS Ctlg	rs796052636

Max Magnitude

0

ClinVar
Risk	rs796052636(A;A)
Alt	rs796052636(A;A)
Reference	Rs796052636(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62071034C>G; NC_000020.10:g.62071034C>T
CLNSRC
CLNACC	RCV000494319.1, RCV000187881.2,