F5 rs6025(PMID:15077257)

SNP information:
Gene ID:2153
Genotype:G/A
Functional Consequence:missense
Global MAF:T=0.0060/30
DNA change:c.1601G
Description:coagulation factor V
Chromosome:1:169549811
Article information:
Method:PCR
Population:Italian Case:Control = 118:132
Related disease:Behcet's disease (BD) Year:2004
Allele/Genotype Case Freq.Case Control Freq.Control OR(95%CI) P value Pc value
AA 0 0
GA 9 0.076 5 0.038 NS
GG 109 0.924 127 0.962 NS
A 9 0.038 5 0.019 1.4 NS
G 227 0.962 259 0.981 0.7 NS
Allele/Genotype with deep vein thrombosis (N=27) Freq.Case Control Freq.Control OR P value Pc value
AA
GA
GG
A 2 0.037 5 0.019 NS
G 52 0.96 259 0.981 NS
Allele/Genotype without deep vein thrombosis (N=91) Freq.Case Control Freq.Control OR P value Pc value
AA
GA
GG
A 16 0.088 5 0.019 NS
G 166 0.912 259 0.981 NS
Allele/Genotype with deep vein thrombosis (N=27) Freq.Case without deep vein thrombosis (N=91) Freq.Control OR P value Pc value
AA
GA
GG
A 2 0.037 16 0.088 NS
G 52 0.96 166 0.912 NS
Function:Undone
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