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rs199472896

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472896(A;A)
Make rs199472896(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952705
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472896
ebirs199472896
HLIrs199472896
Exacrs199472896
Varsomers199472896
Maprs199472896
PheGenIrs199472896
hapmaprs199472896
1000 genomesrs199472896
hgdprs199472896
ensemblrs199472896
gopubmedrs199472896
geneviewrs199472896
scholarrs199472896
googlers199472896
pharmgkbrs199472896
gwascentralrs199472896
openSNPrs199472896
23andMers199472896
23andMe allrs199472896
SNP Nexus

SNPshotrs199472896
SNPdbers199472896
MSV3drs199472896
GWAS Ctlgrs199472896
Max Magnitude0
ClinVar
Risk rs199472896(A;A)
Alt rs199472896(A;A)
Reference rs199472896(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.150649793G>T
CLNSRC ClinVar
CLNACC RCV000057882.2,