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rs199473004

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473004(A;G)
Make rs199473004(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948938
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473004
ebirs199473004
HLIrs199473004
Exacrs199473004
Varsomers199473004
Maprs199473004
PheGenIrs199473004
hapmaprs199473004
1000 genomesrs199473004
hgdprs199473004
ensemblrs199473004
gopubmedrs199473004
geneviewrs199473004
scholarrs199473004
googlers199473004
pharmgkbrs199473004
gwascentralrs199473004
openSNPrs199473004
23andMers199473004
23andMe allrs199473004
SNP Nexus

SNPshotrs199473004
SNPdbers199473004
MSV3drs199473004
GWAS Ctlgrs199473004
Max Magnitude0
ClinVar
Risk rs199473004(G;G)
Alt rs199473004(G;G)
Reference rs199473004(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150646026T>C
CLNSRC ClinVar
CLNACC RCV000058131.2, RCV000181873.1,