UVEOGENE Database

SNP information:

Gene ID:2147
Genotype:G/A
Functional Consequence:downstream variant 500B,utr variant 3 prime
Global MAF:A=0.0036/18
DNA change:c.*97G>A
Description:coagulation factor II, thrombin
Chromosome:11:46739505

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	8	0.068	5	0.038		NS
GG	109	0.932	127	0.962		NS
A	8	0.034	5	0.019	1.3	NS
G	226	0.966	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	4	0.074	5	0.019		NS
G	50	0.926	259	0.981		NS
Allele/Genotype	without deep vein thrombosis (N=91)	Freq.Case	Control	Freq.Control	OR	P value	Pc value
AA
AG
GG
A	12	0.067	5	0.019		NS
G	168	0.933	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
AG
GG
A	4	0.074	12	0.067		NS
G	50	0.926	168	0.933		NS

Function:Undone

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