rs786202724, MET

N. diseases: 5
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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 0.700 1.000 6 1999 2013
Type 1 Papillary Renal Cell Carcinoma
CUI: C1336839
Disease: Type 1 Papillary Renal Cell Carcinoma
14 0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 0.700 1.000 5 1997 1999
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 0.700 1.000 1 1999 1999
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 0.700 1.000 1 2007 2007
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 0.700 0