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rs199473434

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473434(C;T)
Make rs199473434(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948452
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473434
ebirs199473434
HLIrs199473434
Exacrs199473434
Varsomers199473434
Maprs199473434
PheGenIrs199473434
hapmaprs199473434
1000 genomesrs199473434
hgdprs199473434
ensemblrs199473434
gopubmedrs199473434
geneviewrs199473434
scholarrs199473434
googlers199473434
pharmgkbrs199473434
gwascentralrs199473434
openSNPrs199473434
23andMers199473434
23andMe allrs199473434
SNP Nexus

SNPshotrs199473434
SNPdbers199473434
MSV3drs199473434
GWAS Ctlgrs199473434
Max Magnitude0
ClinVar
Risk rs199473434(G,T;G,T)
Alt rs199473434(G,T;G,T)
Reference rs199473434(C;C)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME
Variation info
Gene KCNH2
CLNDBN SUDDEN INFANT DEATH SYNDROME
Reversed 1
HGVS NC_000007.13:g.150645540G>A
CLNSRC ClinVar
CLNACC RCV000058151.2,