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rs199473537

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473537(C;C)
Make rs199473537(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948996
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473537
ebirs199473537
HLIrs199473537
Exacrs199473537
Varsomers199473537
Maprs199473537
PheGenIrs199473537
hapmaprs199473537
1000 genomesrs199473537
hgdprs199473537
ensemblrs199473537
gopubmedrs199473537
geneviewrs199473537
scholarrs199473537
googlers199473537
pharmgkbrs199473537
gwascentralrs199473537
openSNPrs199473537
23andMers199473537
23andMe allrs199473537
SNP Nexus

SNPshotrs199473537
SNPdbers199473537
MSV3drs199473537
GWAS Ctlgrs199473537
Max Magnitude0
ClinVar
Risk rs199473537(C;C)
Alt rs199473537(C;C)
Reference rs199473537(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150646084A>G
CLNSRC ClinVar
CLNACC RCV000058122.2,