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rs199473413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473413(A;A)
Make rs199473413(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974846
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473413
ebirs199473413
HLIrs199473413
Exacrs199473413
Varsomers199473413
Maprs199473413
PheGenIrs199473413
hapmaprs199473413
1000 genomesrs199473413
hgdprs199473413
ensemblrs199473413
gopubmedrs199473413
geneviewrs199473413
scholarrs199473413
googlers199473413
pharmgkbrs199473413
gwascentralrs199473413
openSNPrs199473413
23andMers199473413
23andMe allrs199473413
SNP Nexus

SNPshotrs199473413
SNPdbers199473413
MSV3drs199473413
GWAS Ctlgrs199473413
Max Magnitude0
ClinVar
Risk rs199473413(A;A)
Alt rs199473413(A;A)
Reference rs199473413(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671934C>T
CLNSRC ClinVar
CLNACC RCV000057966.2,