rs143072395

Orientation

plus

Stabilized

plus

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

Make rs143072395(A;A)

Make rs143072395(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150950366

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs143072395
dbSNP (classic)	rs143072395
ClinGen	rs143072395
ebi	rs143072395
HLI	rs143072395
Exac	rs143072395
Gnomad	rs143072395
Varsome	rs143072395
LitVar	rs143072395
Map	rs143072395
PheGenI	rs143072395
Biobank	rs143072395
1000 genomes	rs143072395
hgdp	rs143072395
ensembl	rs143072395
geneview	rs143072395
scholar	rs143072395
google	rs143072395
pharmgkb	rs143072395
gwascentral	rs143072395
openSNP	rs143072395
23andMe	rs143072395
SNPshot	rs143072395
SNPdbe	rs143072395
MSV3d	rs143072395
GWAS Ctlg	rs143072395

Max Magnitude

0

ClinVar
Risk	rs143072395(A;A)
Alt	rs143072395(A;A)
Reference	Rs143072395(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	KCNH2
CLNDBN	not specified
Reversed	0
HGVS	NC_000007.13:g.150647454G>A
CLNSRC
CLNACC	RCV000182043.3,