rs1057518151

Orientation

minus

Stabilized

minus

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

Make rs1057518151(G;T)

Make rs1057518151(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150947327

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057518151
dbSNP (classic)	rs1057518151
ClinGen	rs1057518151
ebi	rs1057518151
HLI	rs1057518151
Exac	rs1057518151
Gnomad	rs1057518151
Varsome	rs1057518151
LitVar	rs1057518151
Map	rs1057518151
PheGenI	rs1057518151
Biobank	rs1057518151
1000 genomes	rs1057518151
hgdp	rs1057518151
ensembl	rs1057518151
geneview	rs1057518151
scholar	rs1057518151
google	rs1057518151
pharmgkb	rs1057518151
gwascentral	rs1057518151
openSNP	rs1057518151
23andMe	rs1057518151
SNPshot	rs1057518151
SNPdbe	rs1057518151
MSV3d	rs1057518151
GWAS Ctlg	rs1057518151

Max Magnitude

0

ClinVar
Risk	rs1057518151(T;T)
Alt	rs1057518151(T;T)
Reference	Rs1057518151(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150644415C>A
CLNSRC
CLNACC	RCV000414266.1,