Have questions? Visit https://www.reddit.com/r/SNPedia

rs199474665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199474665(C;C)
Make rs199474665(C;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position3290
GeneDDX27
is asnp
is mentioned by
dbSNPrs199474665
ebirs199474665
HLIrs199474665
Exacrs199474665
Varsomers199474665
Maprs199474665
PheGenIrs199474665
hapmaprs199474665
1000 genomesrs199474665
hgdprs199474665
ensemblrs199474665
gopubmedrs199474665
geneviewrs199474665
scholarrs199474665
googlers199474665
pharmgkbrs199474665
gwascentralrs199474665
openSNPrs199474665
23andMers199474665
23andMe allrs199474665
SNP Nexus

SNPshotrs199474665
SNPdbers199474665
MSV3drs199474665
GWAS Ctlgrs199474665
GMAF0.001871
Max Magnitude0
ClinVar
Risk rs199474665(C;C)
Alt rs199474665(C;C)
Reference rs199474665(T;T)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME
Variation info
Gene
CLNDBN SUDDEN INFANT DEATH SYNDROME
Reversed 0
HGVS NC_012920.1:m.3290T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010220.2,