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rs189014161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs189014161(C;C)
Make rs189014161(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position150950336
GeneKCNH2
is asnp
is mentioned by
dbSNPrs189014161
dbSNP (old)rs189014161
ClinGenrs189014161
ebirs189014161
HLIrs189014161
Exacrs189014161
Gnomadrs189014161
Varsomers189014161
Maprs189014161
PheGenIrs189014161
Biobankrs189014161
1000 genomesrs189014161
hgdprs189014161
ensemblrs189014161
gopubmedrs189014161
geneviewrs189014161
scholarrs189014161
googlers189014161
pharmgkbrs189014161
gwascentralrs189014161
openSNPrs189014161
23andMers189014161
23andMe allrs189014161
SNP Nexus

SNPshotrs189014161
SNPdbers189014161
MSV3drs189014161
GWAS Ctlgrs189014161
Max Magnitude0
ClinVar
Risk rs189014161(A;A) rs189014161(C;C) rs189014161(T;T)
Alt rs189014161(A;A) rs189014161(C;C) rs189014161(T;T)
Reference Rs189014161(G;G)
Significance Pathogenic
Disease Long QT syndrome 2 not provided Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Long QT syndrome 2 not provided Long QT syndrome
Reversed 0
HGVS NC_000007.13:g.150647424G>A
CLNSRC
CLNACC RCV000157266.1, RCV000181843.2, RCV000473013.1,