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rs199473036

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473036(A;T)
Make rs199473036(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150977913
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473036
ebirs199473036
HLIrs199473036
Exacrs199473036
Varsomers199473036
Maprs199473036
PheGenIrs199473036
hapmaprs199473036
1000 genomesrs199473036
hgdprs199473036
ensemblrs199473036
gopubmedrs199473036
geneviewrs199473036
scholarrs199473036
googlers199473036
pharmgkbrs199473036
gwascentralrs199473036
openSNPrs199473036
23andMers199473036
23andMe allrs199473036
SNP Nexus

SNPshotrs199473036
SNPdbers199473036
MSV3drs199473036
GWAS Ctlgrs199473036
Max Magnitude0
ClinVar
Risk rs199473036(T;T)
Alt rs199473036(T;T)
Reference rs199473036(A;A)
Significance Probable-Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150675001T>A
CLNSRC ClinVar
CLNACC RCV000058074.2,