rs201268831

Orientation

plus

Stabilized

plus

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

Make rs201268831(A;A)

Make rs201268831(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150952652

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs201268831
dbSNP (classic)	rs201268831
ClinGen	rs201268831
ebi	rs201268831
HLI	rs201268831
Exac	rs201268831
Gnomad	rs201268831
Varsome	rs201268831
LitVar	rs201268831
Map	rs201268831
PheGenI	rs201268831
Biobank	rs201268831
1000 genomes	rs201268831
hgdp	rs201268831
ensembl	rs201268831
geneview	rs201268831
scholar	rs201268831
google	rs201268831
pharmgkb	rs201268831
gwascentral	rs201268831
openSNP	rs201268831
23andMe	rs201268831
SNPshot	rs201268831
SNPdbe	rs201268831
MSV3d	rs201268831
GWAS Ctlg	rs201268831

Max Magnitude

0

ClinVar
Risk	rs201268831(A;A) rs201268831(T;T)
Alt	rs201268831(A;A) rs201268831(T;T)
Reference	Rs201268831(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.150649740C>A; NC_000007.13:g.150649740C>T
CLNSRC
CLNACC	RCV000181788.2, RCV000171665.1,