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rs199472879

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472879(A;A)
Make rs199472879(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958140
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472879
ebirs199472879
HLIrs199472879
Exacrs199472879
Varsomers199472879
Maprs199472879
PheGenIrs199472879
hapmaprs199472879
1000 genomesrs199472879
hgdprs199472879
ensemblrs199472879
gopubmedrs199472879
geneviewrs199472879
scholarrs199472879
googlers199472879
pharmgkbrs199472879
gwascentralrs199472879
openSNPrs199472879
23andMers199472879
23andMe allrs199472879
SNP Nexus

SNPshotrs199472879
SNPdbers199472879
MSV3drs199472879
GWAS Ctlgrs199472879
Max Magnitude0
ClinVar
Risk rs199472879(A;A)
Alt rs199472879(A;A)
Reference rs199472879(G;G)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME
Variation info
Gene KCNH2
CLNDBN SUDDEN INFANT DEATH SYNDROME
Reversed 1
HGVS NC_000007.13:g.150655228C>T
CLNSRC ClinVar
CLNACC RCV000058263.2,