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rs199473546

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473546(A;G)
Make rs199473546(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150945502
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473546
ebirs199473546
HLIrs199473546
Exacrs199473546
Varsomers199473546
Maprs199473546
PheGenIrs199473546
hapmaprs199473546
1000 genomesrs199473546
hgdprs199473546
ensemblrs199473546
gopubmedrs199473546
geneviewrs199473546
scholarrs199473546
googlers199473546
pharmgkbrs199473546
gwascentralrs199473546
openSNPrs199473546
23andMers199473546
23andMe allrs199473546
SNP Nexus

SNPshotrs199473546
SNPdbers199473546
MSV3drs199473546
GWAS Ctlgrs199473546
Max Magnitude0
ClinVar
Risk rs199473546(G;G)
Alt rs199473546(G;G)
Reference rs199473546(A;A)
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.150642590T>C
CLNSRC ClinVar
CLNACC RCV000058219.2, RCV000181916.1,