rs7023329, MTAP

N. diseases: 8
Source: BEFREE ×
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.
melanoma
CUI: C0025202
Disease: melanoma
352 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.810 1.000 1 2009 2017
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
102 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.010 1.000 1 2013 2013
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.010 1.000 1 2013 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.010 1.000 1 2011 2011
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
155 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.010 1.000 1 2013 2013
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.010 1.000 1 2011 2011
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
320 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.010 1.000 1 2017 2017