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rs483223

From SNPedia

Orientationminus
Stabilizedminus
Make rs483223(C;C)
Make rs483223(C;T)
Make rs483223(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position117299200
GeneROS1
is asnp
is mentioned by
dbSNPrs483223
ebirs483223
HLIrs483223
Exacrs483223
Varsomers483223
Maprs483223
PheGenIrs483223
hapmaprs483223
1000 genomesrs483223
hgdprs483223
ensemblrs483223
gopubmedrs483223
geneviewrs483223
scholarrs483223
googlers483223
pharmgkbrs483223
gwascentralrs483223
openSNPrs483223
23andMers483223
23andMe allrs483223
SNP Nexus

SNPshotrs483223
SNPdbers483223
MSV3drs483223
GWAS Ctlgrs483223
GMAF0.1593
Max Magnitude
? (C;C) (C;T) (T;T) 28
Rs483223
PubMed [PMID 16175505OA-icon.png]
Affy Probeset SNP_A-8674727
Affy Orientation same
On GW 5.0 0
Alleles A/B C/T
Ancestral T
Population Caucasian
Allele T
Case Freq.
Control Freq.
Odds Ratio Het 1.15
Odds Ratio Hom 1.75
Odds Ratio All
Disease Myocardial Infarction (MI)


rs483223 is in linkage disequilibrium with a polymorphism that increases susceptibility to Myocardial Infarction 1.15 times for heterozygotes (CT) and 1.75 times for homozygotes (TT) [PMID 16175505OA-icon.png]