rs1057518169

Orientation

minus

Stabilized

minus

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

Make rs1057518169(C;C)

Make rs1057518169(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150947326

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057518169
dbSNP (classic)	rs1057518169
ClinGen	rs1057518169
ebi	rs1057518169
HLI	rs1057518169
Exac	rs1057518169
Gnomad	rs1057518169
Varsome	rs1057518169
LitVar	rs1057518169
Map	rs1057518169
PheGenI	rs1057518169
Biobank	rs1057518169
1000 genomes	rs1057518169
hgdp	rs1057518169
ensembl	rs1057518169
geneview	rs1057518169
scholar	rs1057518169
google	rs1057518169
pharmgkb	rs1057518169
gwascentral	rs1057518169
openSNP	rs1057518169
23andMe	rs1057518169
SNPshot	rs1057518169
SNPdbe	rs1057518169
MSV3d	rs1057518169
GWAS Ctlg	rs1057518169

Max Magnitude

0

ClinVar
Risk	rs1057518169(C;C)
Alt	rs1057518169(C;C)
Reference	Rs1057518169(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150644414A>G
CLNSRC
CLNACC	RCV000413963.1,