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rs199473490

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473490(G;T)
Make rs199473490(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974878
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473490
ebirs199473490
HLIrs199473490
Exacrs199473490
Varsomers199473490
Maprs199473490
PheGenIrs199473490
hapmaprs199473490
1000 genomesrs199473490
hgdprs199473490
ensemblrs199473490
gopubmedrs199473490
geneviewrs199473490
scholarrs199473490
googlers199473490
pharmgkbrs199473490
gwascentralrs199473490
openSNPrs199473490
23andMers199473490
23andMe allrs199473490
SNP Nexus

SNPshotrs199473490
SNPdbers199473490
MSV3drs199473490
GWAS Ctlgrs199473490
Max Magnitude0
ClinVar
Risk rs199473490(T;T)
Alt rs199473490(T;T)
Reference rs199473490(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671966C>A
CLNSRC ClinVar
CLNACC RCV000057903.2,