rs796052670

Orientation

minus

Stabilized

minus

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

Make rs796052670(G;T)

Make rs796052670(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63408412

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052670
dbSNP (classic)	rs796052670
ClinGen	rs796052670
ebi	rs796052670
HLI	rs796052670
Exac	rs796052670
Gnomad	rs796052670
Varsome	rs796052670
LitVar	rs796052670
Map	rs796052670
PheGenI	rs796052670
Biobank	rs796052670
1000 genomes	rs796052670
hgdp	rs796052670
ensembl	rs796052670
geneview	rs796052670
scholar	rs796052670
google	rs796052670
pharmgkb	rs796052670
gwascentral	rs796052670
openSNP	rs796052670
23andMe	rs796052670
SNPshot	rs796052670
SNPdbe	rs796052670
MSV3d	rs796052670
GWAS Ctlg	rs796052670

Max Magnitude

0

ClinVar
Risk	rs796052670(T;T)
Alt	rs796052670(T;T)
Reference	Rs796052670(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62039765C>A
CLNSRC
CLNACC	RCV000187954.1,