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rs199473029

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473029(A;G)
Make rs199473029(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150946974
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473029
ebirs199473029
HLIrs199473029
Exacrs199473029
Varsomers199473029
Maprs199473029
PheGenIrs199473029
hapmaprs199473029
1000 genomesrs199473029
hgdprs199473029
ensemblrs199473029
gopubmedrs199473029
geneviewrs199473029
scholarrs199473029
googlers199473029
pharmgkbrs199473029
gwascentralrs199473029
openSNPrs199473029
23andMers199473029
23andMe allrs199473029
SNP Nexus

SNPshotrs199473029
SNPdbers199473029
MSV3drs199473029
GWAS Ctlgrs199473029
Max Magnitude0
ClinVar
Risk rs199473029(G;G)
Alt rs199473029(G;G)
Reference rs199473029(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150644062T>C
CLNSRC ClinVar
CLNACC RCV000058212.2,