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rs199472877

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472877(A;A)
Make rs199472877(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958157
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472877
ebirs199472877
HLIrs199472877
Exacrs199472877
Varsomers199472877
Maprs199472877
PheGenIrs199472877
hapmaprs199472877
1000 genomesrs199472877
hgdprs199472877
ensemblrs199472877
gopubmedrs199472877
geneviewrs199472877
scholarrs199472877
googlers199472877
pharmgkbrs199472877
gwascentralrs199472877
openSNPrs199472877
23andMers199472877
23andMe allrs199472877
SNP Nexus

SNPshotrs199472877
SNPdbers199472877
MSV3drs199472877
GWAS Ctlgrs199472877
Max Magnitude0
ClinVar
Risk rs199472877(A;A)
Alt rs199472877(A;A)
Reference rs199472877(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.150655245C>T
CLNSRC ClinVar
CLNACC RCV000058260.2,