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rs199472861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472861(C;T)
Make rs199472861(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150959704
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472861
ebirs199472861
HLIrs199472861
Exacrs199472861
Varsomers199472861
Maprs199472861
PheGenIrs199472861
hapmaprs199472861
1000 genomesrs199472861
hgdprs199472861
ensemblrs199472861
gopubmedrs199472861
geneviewrs199472861
scholarrs199472861
googlers199472861
pharmgkbrs199472861
gwascentralrs199472861
openSNPrs199472861
23andMers199472861
23andMe allrs199472861
SNP Nexus

SNPshotrs199472861
SNPdbers199472861
MSV3drs199472861
GWAS Ctlgrs199472861
Max Magnitude0
ClinVar
Risk rs199472861(T;T)
Alt rs199472861(T;T)
Reference rs199472861(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150656792G>A
CLNSRC ClinVar
CLNACC RCV000058223.2,