rs765427343

Orientation

plus

Stabilized

plus

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

Make rs765427343(A;C)

Make rs765427343(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150948471

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs765427343
dbSNP (classic)	rs765427343
ClinGen	rs765427343
ebi	rs765427343
HLI	rs765427343
Exac	rs765427343
Gnomad	rs765427343
Varsome	rs765427343
LitVar	rs765427343
Map	rs765427343
PheGenI	rs765427343
Biobank	rs765427343
1000 genomes	rs765427343
hgdp	rs765427343
ensembl	rs765427343
geneview	rs765427343
scholar	rs765427343
google	rs765427343
pharmgkb	rs765427343
gwascentral	rs765427343
openSNP	rs765427343
23andMe	rs765427343
SNPshot	rs765427343
SNPdbe	rs765427343
MSV3d	rs765427343
GWAS Ctlg	rs765427343

Max Magnitude

0

ClinVar
Risk	rs765427343(C;C) rs765427343(T;T)
Alt	rs765427343(C;C) rs765427343(T;T)
Reference	Rs765427343(A;A)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	KCNH2
CLNDBN	not specified
Reversed	0
HGVS	NC_000007.13:g.150645559A>C
CLNSRC
CLNACC	RCV000181878.2,