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rs199472960

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472960(A;G)
Make rs199472960(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951496
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472960
ebirs199472960
HLIrs199472960
Exacrs199472960
Varsomers199472960
Maprs199472960
PheGenIrs199472960
hapmaprs199472960
1000 genomesrs199472960
hgdprs199472960
ensemblrs199472960
gopubmedrs199472960
geneviewrs199472960
scholarrs199472960
googlers199472960
pharmgkbrs199472960
gwascentralrs199472960
openSNPrs199472960
23andMers199472960
23andMe allrs199472960
SNP Nexus

SNPshotrs199472960
SNPdbers199472960
MSV3drs199472960
GWAS Ctlgrs199472960
Max Magnitude0
ClinVar
Risk rs199472960(G;G)
Alt rs199472960(G;G)
Reference rs199472960(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.150648584T>C
CLNSRC ClinVar
CLNACC RCV000058041.2,