rs796052664

Orientation

minus

Stabilized

minus

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

Make rs796052664(CCT;CCT)

Make rs796052664(CCT;TC)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63439649

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs796052664
dbSNP (classic)	rs796052664
ClinGen	rs796052664
ebi	rs796052664
HLI	rs796052664
Exac	rs796052664
Gnomad	rs796052664
Varsome	rs796052664
LitVar	rs796052664
Map	rs796052664
PheGenI	rs796052664
Biobank	rs796052664
1000 genomes	rs796052664
hgdp	rs796052664
ensembl	rs796052664
geneview	rs796052664
scholar	rs796052664
google	rs796052664
pharmgkb	rs796052664
gwascentral	rs796052664
openSNP	rs796052664
23andMe	rs796052664
SNPshot	rs796052664
SNPdbe	rs796052664
MSV3d	rs796052664
GWAS Ctlg	rs796052664

Max Magnitude

0

ClinVar
Risk	rs796052664(CCT;CCT)
Alt	rs796052664(CCT;CCT)
Reference	Rs796052664(TC;TC)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62071002_62071003delGAinsAGG
CLNSRC
CLNACC	RCV000187943.1,