rs1057518089

Orientation

minus

Stabilized

minus

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

Make rs1057518089(-;T)

Make rs1057518089(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150947006

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057518089
dbSNP (classic)	rs1057518089
ClinGen	rs1057518089
ebi	rs1057518089
HLI	rs1057518089
Exac	rs1057518089
Gnomad	rs1057518089
Varsome	rs1057518089
LitVar	rs1057518089
Map	rs1057518089
PheGenI	rs1057518089
Biobank	rs1057518089
1000 genomes	rs1057518089
hgdp	rs1057518089
ensembl	rs1057518089
geneview	rs1057518089
scholar	rs1057518089
google	rs1057518089
pharmgkb	rs1057518089
gwascentral	rs1057518089
openSNP	rs1057518089
23andMe	rs1057518089
SNPshot	rs1057518089
SNPdbe	rs1057518089
MSV3d	rs1057518089
GWAS Ctlg	rs1057518089

Max Magnitude

0

ClinVar
Risk	rs1057518089(T;T)
Alt	rs1057518089(T;T)
Reference	Rs1057518089(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150644095dupA
CLNSRC
CLNACC	RCV000414739.1,