rs771674303

Orientation

plus

Stabilized

plus

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

Make rs771674303(A;A)

Make rs771674303(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150950240

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs771674303
dbSNP (classic)	rs771674303
ClinGen	rs771674303
ebi	rs771674303
HLI	rs771674303
Exac	rs771674303
Gnomad	rs771674303
Varsome	rs771674303
LitVar	rs771674303
Map	rs771674303
PheGenI	rs771674303
Biobank	rs771674303
1000 genomes	rs771674303
hgdp	rs771674303
ensembl	rs771674303
geneview	rs771674303
scholar	rs771674303
google	rs771674303
pharmgkb	rs771674303
gwascentral	rs771674303
openSNP	rs771674303
23andMe	rs771674303
SNPshot	rs771674303
SNPdbe	rs771674303
MSV3d	rs771674303
GWAS Ctlg	rs771674303

Max Magnitude

0

ClinVar
Risk	rs771674303(A;A) rs771674303(T;T)
Alt	rs771674303(A;A) rs771674303(T;T)
Reference	Rs771674303(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.150647328G>A
CLNSRC
CLNACC	RCV000181847.1,