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rs199473549

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473549(G;T)
Make rs199473549(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958094
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473549
ebirs199473549
HLIrs199473549
Exacrs199473549
Varsomers199473549
Maprs199473549
PheGenIrs199473549
hapmaprs199473549
1000 genomesrs199473549
hgdprs199473549
ensemblrs199473549
gopubmedrs199473549
geneviewrs199473549
scholarrs199473549
googlers199473549
pharmgkbrs199473549
gwascentralrs199473549
openSNPrs199473549
23andMers199473549
23andMe allrs199473549
SNP Nexus

SNPshotrs199473549
SNPdbers199473549
MSV3drs199473549
GWAS Ctlgrs199473549
Max Magnitude0
ClinVar
Risk rs199473549(T;T)
Alt rs199473549(T;T)
Reference rs199473549(G;G)
Significance Probable-Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME
Variation info
Gene KCNH2
CLNDBN SUDDEN INFANT DEATH SYNDROME
Reversed 1
HGVS NC_000007.13:g.150655182C>A
CLNSRC ClinVar
CLNACC RCV000058268.2,