rs1057520558

Orientation

minus

Stabilized

minus

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

Make rs1057520558(C;G)

Make rs1057520558(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150947453

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057520558
dbSNP (classic)	rs1057520558
ClinGen	rs1057520558
ebi	rs1057520558
HLI	rs1057520558
Exac	rs1057520558
Gnomad	rs1057520558
Varsome	rs1057520558
LitVar	rs1057520558
Map	rs1057520558
PheGenI	rs1057520558
Biobank	rs1057520558
1000 genomes	rs1057520558
hgdp	rs1057520558
ensembl	rs1057520558
geneview	rs1057520558
scholar	rs1057520558
google	rs1057520558
pharmgkb	rs1057520558
gwascentral	rs1057520558
openSNP	rs1057520558
23andMe	rs1057520558
SNPshot	rs1057520558
SNPdbe	rs1057520558
MSV3d	rs1057520558
GWAS Ctlg	rs1057520558

Max Magnitude

0

ClinVar
Risk	rs1057520558(G;G)
Alt	rs1057520558(G;G)
Reference	Rs1057520558(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150644541G>C
CLNSRC
CLNACC	RCV000423718.1,