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rs199472866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472866(A;A)
Make rs199472866(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958484
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472866
ebirs199472866
HLIrs199472866
Exacrs199472866
Varsomers199472866
Maprs199472866
PheGenIrs199472866
hapmaprs199472866
1000 genomesrs199472866
hgdprs199472866
ensemblrs199472866
gopubmedrs199472866
geneviewrs199472866
scholarrs199472866
googlers199472866
pharmgkbrs199472866
gwascentralrs199472866
openSNPrs199472866
23andMers199472866
23andMe allrs199472866
SNP Nexus

SNPshotrs199472866
SNPdbers199472866
MSV3drs199472866
GWAS Ctlgrs199472866
Max Magnitude0
ClinVar
Risk rs199472866(A;A)
Alt rs199472866(A;A)
Reference rs199472866(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome 2
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Long QT syndrome 2
Reversed 1
HGVS NC_000007.13:g.150655572C>T
CLNSRC ClinVar
CLNACC RCV000058237.2, RCV000202703.1,