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rs1057520598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520598(A;G)
Make rs1057520598(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150959738
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057520598
dbSNP (old)rs1057520598
ClinGenrs1057520598
ebirs1057520598
HLIrs1057520598
Exacrs1057520598
Gnomadrs1057520598
Varsomers1057520598
Maprs1057520598
PheGenIrs1057520598
Biobankrs1057520598
1000 genomesrs1057520598
hgdprs1057520598
ensemblrs1057520598
gopubmedrs1057520598
geneviewrs1057520598
scholarrs1057520598
googlers1057520598
pharmgkbrs1057520598
gwascentralrs1057520598
openSNPrs1057520598
23andMers1057520598
23andMe allrs1057520598
SNPshotrs1057520598
SNPdbers1057520598
MSV3drs1057520598
GWAS Ctlgrs1057520598
Max Magnitude0
ClinVar
Risk rs1057520598(G;G)
Alt rs1057520598(G;G)
Reference Rs1057520598(A;A)
Significance Pathogenic
Disease not provided Long QT syndrome
Variation info
Gene KCNH2
CLNDBN not provided Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150656826T>C
CLNSRC
CLNACC RCV000427208.1, RCV000460573.1,