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: rs2816958
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.800 1.000 4 2012 2017
dbSNP: rs3790844
rs3790844
NR5A2
0.882 0.200 1 200038304 intron variant A/C;G snv
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.730 1.000 2 2010 2018
dbSNP: rs2816958
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 2 2015 2017
dbSNP: rs12131072
rs12131072
NR5A2
1 200088375 intron variant C/A;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs1986405
rs1986405
NR5A2
1 200126807 intron variant C/G;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs2690034
rs2690034
NR5A2
1 200174716 3 prime UTR variant C/G snv 0.65
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2816958
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs2816958
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs2816958
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs2816958
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs2816992
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs2816992
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2816992
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs2816992
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs2821332
rs2821332
NR5A2
1 200116586 intron variant T/A snv 0.41
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2018 2018
dbSNP: rs2821391
rs2821391
NR5A2
1 200067662 intron variant A/G snv 0.36
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
dbSNP: rs6658424
rs6658424
NR5A2
1 200080174 intron variant T/A snv 0.29
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019