rs11125529, ACYP2

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Chronic osteomyelitis
CUI: C0008707
Disease: Chronic osteomyelitis
12 0.882 0.280 2 54248729 intron variant C/A;T snv 0.700 0
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
CUI: C1832661
Disease: ANOPHTHALMIA AND PULMONARY HYPOPLASIA
80 0.882 0.280 2 54248729 intron variant C/A;T snv 0.010 1.000 1 2019 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.882 0.280 2 54248729 intron variant C/A;T snv 0.010 1.000 1 2017 2017