rs1057522921

Orientation

minus

Stabilized

minus

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

Make rs1057522921(G;T)

Make rs1057522921(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150948439

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057522921
dbSNP (classic)	rs1057522921
ClinGen	rs1057522921
ebi	rs1057522921
HLI	rs1057522921
Exac	rs1057522921
Gnomad	rs1057522921
Varsome	rs1057522921
LitVar	rs1057522921
Map	rs1057522921
PheGenI	rs1057522921
Biobank	rs1057522921
1000 genomes	rs1057522921
hgdp	rs1057522921
ensembl	rs1057522921
geneview	rs1057522921
scholar	rs1057522921
google	rs1057522921
pharmgkb	rs1057522921
gwascentral	rs1057522921
openSNP	rs1057522921
23andMe	rs1057522921
SNPshot	rs1057522921
SNPdbe	rs1057522921
MSV3d	rs1057522921
GWAS Ctlg	rs1057522921

Max Magnitude

0

ClinVar
Risk	rs1057522921(T;T)
Alt	rs1057522921(T;T)
Reference	Rs1057522921(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150645527C>A
CLNSRC
CLNACC	RCV000418102.1,