rs132985, PLA2G6

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.
melanoma
CUI: C0025202
Disease: melanoma
515 0.827 0.120 22 38167464 intron variant C/T snv 0.51 0.710 1.000 2 2009 2012
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.827 0.120 22 38167464 intron variant C/T snv 0.51 0.700 1.000 1 2018 2018
Malignant melanoma of skin of lower limb
42 0.827 0.120 22 38167464 intron variant C/T snv 0.51 0.700 1.000 1 2018 2018
Malignant melanoma of skin of upper limb
42 0.827 0.120 22 38167464 intron variant C/T snv 0.51 0.700 1.000 1 2018 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.827 0.120 22 38167464 intron variant C/T snv 0.51 0.010 1.000 1 2012 2012