rs1057519853, GNAQ

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.
Uveal melanoma
CUI: C0220633
Disease: Uveal melanoma
22 0.851 0.080 9 77794572 missense variant TG/AA mnv 0.740 0.800 5 2014 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.851 0.080 9 77794572 missense variant TG/AA mnv 0.040 0.750 4 2014 2019
melanoma
CUI: C0025202
Disease: melanoma
515 0.851 0.080 9 77794572 missense variant TG/AA mnv 0.030 1.000 3 2012 2018
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.851 0.080 9 77794572 missense variant TG/AA mnv 0.010 1 2018 2018
Hemangioma
CUI: C0018916
Disease: Hemangioma
24 0.851 0.080 9 77794572 missense variant TG/AA mnv 0.010 1.000 1 2019 2019
Nevus of choroid
CUI: C0346392
Disease: Nevus of choroid
2 0.851 0.080 9 77794572 missense variant TG/AA mnv 0.010 1.000 1 2019 2019