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rs199472873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472873(C;T)
Make rs199472873(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958224
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472873
ebirs199472873
HLIrs199472873
Exacrs199472873
Varsomers199472873
Maprs199472873
PheGenIrs199472873
hapmaprs199472873
1000 genomesrs199472873
hgdprs199472873
ensemblrs199472873
gopubmedrs199472873
geneviewrs199472873
scholarrs199472873
googlers199472873
pharmgkbrs199472873
gwascentralrs199472873
openSNPrs199472873
23andMers199472873
23andMe allrs199472873
SNP Nexus

SNPshotrs199472873
SNPdbers199472873
MSV3drs199472873
GWAS Ctlgrs199472873
Max Magnitude0
ClinVar
Risk rs199472873(G,T;G,T)
Alt rs199472873(G,T;G,T)
Reference rs199472873(C;C)
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.150655312G>A; NC_000007.13:g.150655312G>C
CLNSRC ClinVar
CLNACC RCV000058252.2, RCV000058251.2,