rs786205588

Orientation

minus

Stabilized

minus

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

Make rs786205588(C;C)

Make rs786205588(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951655

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs786205588
dbSNP (classic)	rs786205588
ClinGen	rs786205588
ebi	rs786205588
HLI	rs786205588
Exac	rs786205588
Gnomad	rs786205588
Varsome	rs786205588
LitVar	rs786205588
Map	rs786205588
PheGenI	rs786205588
Biobank	rs786205588
1000 genomes	rs786205588
hgdp	rs786205588
ensembl	rs786205588
geneview	rs786205588
scholar	rs786205588
google	rs786205588
pharmgkb	rs786205588
gwascentral	rs786205588
openSNP	rs786205588
23andMe	rs786205588
SNPshot	rs786205588
SNPdbe	rs786205588
MSV3d	rs786205588
GWAS Ctlg	rs786205588

Max Magnitude

0

ClinVar
Risk	rs786205588(C;C)
Alt	rs786205588(C;C)
Reference	Rs786205588(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648743C>G
CLNSRC
CLNACC	RCV000171410.1,