rs796052635

Orientation

minus

Stabilized

minus

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

Make rs796052635(A;A)

Make rs796052635(A;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63439707

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052635
dbSNP (classic)	rs796052635
ClinGen	rs796052635
ebi	rs796052635
HLI	rs796052635
Exac	rs796052635
Gnomad	rs796052635
Varsome	rs796052635
LitVar	rs796052635
Map	rs796052635
PheGenI	rs796052635
Biobank	rs796052635
1000 genomes	rs796052635
hgdp	rs796052635
ensembl	rs796052635
geneview	rs796052635
scholar	rs796052635
google	rs796052635
pharmgkb	rs796052635
gwascentral	rs796052635
openSNP	rs796052635
23andMe	rs796052635
SNPshot	rs796052635
SNPdbe	rs796052635
MSV3d	rs796052635
GWAS Ctlg	rs796052635

Max Magnitude

0

ClinVar
Risk	rs796052635(A;A)
Alt	rs796052635(A;A)
Reference	Rs796052635(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62071060A>T
CLNSRC
CLNACC	RCV000187880.1,