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: rs8005161
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.810 1.000 2 2012 2019
dbSNP: rs8005161
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 3 2010 2017
dbSNP: rs8005172
rs8005172
GPR65
1.000 0.040 14 88006268 intron variant C/T snv 0.41
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.710 1.000 1 2017 2018
dbSNP: rs8005161
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs8005161
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019