Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 0.800 2 2010 2017
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 1.000 1 2010 2015
dbSNP: rs3024490
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.710 0.500 1 2013 2017