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rs199473002

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473002(C;T)
Make rs199473002(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948971
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473002
ebirs199473002
HLIrs199473002
Exacrs199473002
Varsomers199473002
Maprs199473002
PheGenIrs199473002
hapmaprs199473002
1000 genomesrs199473002
hgdprs199473002
ensemblrs199473002
gopubmedrs199473002
geneviewrs199473002
scholarrs199473002
googlers199473002
pharmgkbrs199473002
gwascentralrs199473002
openSNPrs199473002
23andMers199473002
23andMe allrs199473002
SNP Nexus

SNPshotrs199473002
SNPdbers199473002
MSV3drs199473002
GWAS Ctlgrs199473002
Max Magnitude0
ClinVar
Risk rs199473002(T;T)
Alt rs199473002(T;T)
Reference rs199473002(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000007.13:g.150646059G>A
CLNSRC ClinVar
CLNACC RCV000058127.2, RCV000181868.2,