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rs199472860

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472860(A;T)
Make rs199472860(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150959712
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472860
ebirs199472860
HLIrs199472860
Exacrs199472860
Varsomers199472860
Maprs199472860
PheGenIrs199472860
hapmaprs199472860
1000 genomesrs199472860
hgdprs199472860
ensemblrs199472860
gopubmedrs199472860
geneviewrs199472860
scholarrs199472860
googlers199472860
pharmgkbrs199472860
gwascentralrs199472860
openSNPrs199472860
23andMers199472860
23andMe allrs199472860
SNP Nexus

SNPshotrs199472860
SNPdbers199472860
MSV3drs199472860
GWAS Ctlgrs199472860
Max Magnitude0
ClinVar
Risk rs199472860(T;T)
Alt rs199472860(T;T)
Reference rs199472860(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.150656800T>A
CLNSRC ClinVar
CLNACC RCV000058218.2,