rs796052666

Orientation

minus

Stabilized

minus

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

Make rs796052666(-;T)

Make rs796052666(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63407332

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052666
dbSNP (classic)	rs796052666
ClinGen	rs796052666
ebi	rs796052666
HLI	rs796052666
Exac	rs796052666
Gnomad	rs796052666
Varsome	rs796052666
LitVar	rs796052666
Map	rs796052666
PheGenI	rs796052666
Biobank	rs796052666
1000 genomes	rs796052666
hgdp	rs796052666
ensembl	rs796052666
geneview	rs796052666
scholar	rs796052666
google	rs796052666
pharmgkb	rs796052666
gwascentral	rs796052666
openSNP	rs796052666
23andMe	rs796052666
SNPshot	rs796052666
SNPdbe	rs796052666
MSV3d	rs796052666
GWAS Ctlg	rs796052666

Max Magnitude

0

ClinVar
Risk	rs796052666(T;T)
Alt	rs796052666(T;T)
Reference	Rs796052666(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62038686dupA
CLNSRC
CLNACC	RCV000187945.1,