UVEOGENE Database

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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