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rs199473506

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473506(A;G)
Make rs199473506(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952777
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473506
ebirs199473506
HLIrs199473506
Exacrs199473506
Varsomers199473506
Maprs199473506
PheGenIrs199473506
hapmaprs199473506
1000 genomesrs199473506
hgdprs199473506
ensemblrs199473506
gopubmedrs199473506
geneviewrs199473506
scholarrs199473506
googlers199473506
pharmgkbrs199473506
gwascentralrs199473506
openSNPrs199473506
23andMers199473506
23andMe allrs199473506
SNP Nexus

SNPshotrs199473506
SNPdbers199473506
MSV3drs199473506
GWAS Ctlgrs199473506
Max Magnitude0
ClinVar
Risk rs199473506(G;G)
Alt rs199473506(G;G)
Reference rs199473506(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.150649865T>C
CLNSRC ClinVar
CLNACC RCV000057873.2,