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rs878853771

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853771(A;A)
Make rs878853771(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position150952503
GeneKCNH2
is asnp
is mentioned by
dbSNPrs878853771
ebirs878853771
HLIrs878853771
Exacrs878853771
Varsomers878853771
Maprs878853771
PheGenIrs878853771
hapmaprs878853771
1000 genomesrs878853771
hgdprs878853771
ensemblrs878853771
gopubmedrs878853771
geneviewrs878853771
scholarrs878853771
googlers878853771
pharmgkbrs878853771
gwascentralrs878853771
openSNPrs878853771
23andMers878853771
23andMe allrs878853771
SNP Nexus

SNPshotrs878853771
SNPdbers878853771
MSV3drs878853771
GWAS Ctlgrs878853771
Max Magnitude0
ClinVar
Risk rs878853771(A;A)
Alt rs878853771(A;A)
Reference rs878853771(C;C)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649591G>T
CLNSRC
CLNACC RCV000228054.1,