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rs199472908

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472908(A;A)
Make rs199472908(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952556
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472908
ebirs199472908
HLIrs199472908
Exacrs199472908
Varsomers199472908
Maprs199472908
PheGenIrs199472908
hapmaprs199472908
1000 genomesrs199472908
hgdprs199472908
ensemblrs199472908
gopubmedrs199472908
geneviewrs199472908
scholarrs199472908
googlers199472908
pharmgkbrs199472908
gwascentralrs199472908
openSNPrs199472908
23andMers199472908
23andMe allrs199472908
SNP Nexus

SNPshotrs199472908
SNPdbers199472908
MSV3drs199472908
GWAS Ctlgrs199472908
Max Magnitude0
ClinVar
Risk rs199472908(A;A)
Alt rs199472908(A;A)
Reference rs199472908(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.150649644C>T
CLNSRC ClinVar
CLNACC RCV000057908.2,