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rs199473025

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Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473025(C;T)
Make rs199473025(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947347
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473025
ebirs199473025
HLIrs199473025
Exacrs199473025
Varsomers199473025
Maprs199473025
PheGenIrs199473025
hapmaprs199473025
1000 genomesrs199473025
hgdprs199473025
ensemblrs199473025
gopubmedrs199473025
geneviewrs199473025
scholarrs199473025
googlers199473025
pharmgkbrs199473025
gwascentralrs199473025
openSNPrs199473025
23andMers199473025
23andMe allrs199473025
SNP Nexus

SNPshotrs199473025
SNPdbers199473025
MSV3drs199473025
GWAS Ctlgrs199473025
Max Magnitude0
ClinVar
Risk rs199473025(T;T)
Alt rs199473025(T;T)
Reference rs199473025(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Arrhythmogenic right ventricular cardiomyopathy Primary dilated cardiomyopathy Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Arrhythmogenic right ventricular cardiomyopathy Primary dilated cardiomyopathy Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150644435G>A
CLNSRC ClinVar
CLNACC RCV000058201.2, RCV000143906.1, RCV000143907.1, RCV000157268.1,