rs563611707

Orientation

plus

Stabilized

plus

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

Make rs563611707(A;A)

Make rs563611707(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150974744

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs563611707
dbSNP (classic)	rs563611707
ClinGen	rs563611707
ebi	rs563611707
HLI	rs563611707
Exac	rs563611707
Gnomad	rs563611707
Varsome	rs563611707
LitVar	rs563611707
Map	rs563611707
PheGenI	rs563611707
Biobank	rs563611707
1000 genomes	rs563611707
hgdp	rs563611707
ensembl	rs563611707
geneview	rs563611707
scholar	rs563611707
google	rs563611707
pharmgkb	rs563611707
gwascentral	rs563611707
openSNP	rs563611707
23andMe	rs563611707
SNPshot	rs563611707
SNPdbe	rs563611707
MSV3d	rs563611707
GWAS Ctlg	rs563611707

Max Magnitude

0

ClinVar
Risk	rs563611707(A;A)
Alt	rs563611707(A;A)
Reference	Rs563611707(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	KCNH2
CLNDBN	not specified
Reversed	0
HGVS	NC_000007.13:g.150671832G>A
CLNSRC
CLNACC	RCV000181942.2,