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rs199473426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473426(G;T)
Make rs199473426(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951648
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473426
ebirs199473426
HLIrs199473426
Exacrs199473426
Varsomers199473426
Maprs199473426
PheGenIrs199473426
hapmaprs199473426
1000 genomesrs199473426
hgdprs199473426
ensemblrs199473426
gopubmedrs199473426
geneviewrs199473426
scholarrs199473426
googlers199473426
pharmgkbrs199473426
gwascentralrs199473426
openSNPrs199473426
23andMers199473426
23andMe allrs199473426
SNP Nexus

SNPshotrs199473426
SNPdbers199473426
MSV3drs199473426
GWAS Ctlgrs199473426
Max Magnitude0
ClinVar
Risk rs199473426(A,T;A,T)
Alt rs199473426(A,T;A,T)
Reference rs199473426(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.150648736C>A
CLNSRC ClinVar
CLNACC RCV000057971.2,