Source: GWASCAT

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: rs2284553
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 4 2012 2017
dbSNP: rs2834215
rs2834215
IFNGR2
1.000 0.040 21 33424579 intron variant A/G snv 0.45
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2013 2013
dbSNP: rs2284553
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 2 2015 2017
dbSNP: rs2284553
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs2284553
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs2284553
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs2284553
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs9808753
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs9808753
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015