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rs199473024

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473024(A;G)
Make rs199473024(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947362
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473024
ebirs199473024
HLIrs199473024
Exacrs199473024
Varsomers199473024
Maprs199473024
PheGenIrs199473024
hapmaprs199473024
1000 genomesrs199473024
hgdprs199473024
ensemblrs199473024
gopubmedrs199473024
geneviewrs199473024
scholarrs199473024
googlers199473024
pharmgkbrs199473024
gwascentralrs199473024
openSNPrs199473024
23andMers199473024
23andMe allrs199473024
SNP Nexus

SNPshotrs199473024
SNPdbers199473024
MSV3drs199473024
GWAS Ctlgrs199473024
Max Magnitude0
ClinVar
Risk rs199473024(G;G)
Alt rs199473024(G;G)
Reference rs199473024(A;A)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME
Variation info
Gene KCNH2
CLNDBN SUDDEN INFANT DEATH SYNDROME
Reversed 1
HGVS NC_000007.13:g.150644450T>C
CLNSRC ClinVar
CLNACC RCV000058200.2,