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rs150988911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150988911(C;T)
Make rs150988911(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150959701
GeneKCNH2
is asnp
is mentioned by
dbSNPrs150988911
ebirs150988911
HLIrs150988911
Exacrs150988911
Varsomers150988911
Maprs150988911
PheGenIrs150988911
hapmaprs150988911
1000 genomesrs150988911
hgdprs150988911
ensemblrs150988911
gopubmedrs150988911
geneviewrs150988911
scholarrs150988911
googlers150988911
pharmgkbrs150988911
gwascentralrs150988911
openSNPrs150988911
23andMers150988911
23andMe allrs150988911
SNP Nexus

SNPshotrs150988911
SNPdbers150988911
MSV3drs150988911
GWAS Ctlgrs150988911
Max Magnitude0
ClinVar
Risk rs150988911(T;T)
Alt rs150988911(T;T)
Reference rs150988911(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome 2 Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Long QT syndrome 2 Long QT syndrome
Reversed 0
HGVS NC_000007.13:g.150656789C>T
CLNSRC ClinVar University of Washington
CLNACC RCV000058225.2, RCV000148529.1, RCV000226122.1,