rs121965039, OAT

N. diseases: 6
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.
Gyrate Atrophy
CUI: C0018425
Disease: Gyrate Atrophy
35 0.851 0.160 10 124408601 missense variant C/A;T snv 8.0E-06 0.700 1.000 7 1988 2013
Hyperornithinemia
CUI: C0599035
Disease: Hyperornithinemia
65 0.851 0.160 10 124408601 missense variant C/A;T snv 8.0E-06 0.700 0
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.851 0.160 10 124408601 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2003 2003
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.851 0.160 10 124408601 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2003 2003
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.851 0.160 10 124408601 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2003 2003
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.851 0.160 10 124408601 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2003 2003