rs199498, WNT3;LRRC37A2

N. diseases: 2
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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.925 0.120 17 46788237 intron variant T/C;G snv 0.800 1.000 1 2014 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.925 0.120 17 46788237 intron variant T/C;G snv 0.700 1.000 1 2017 2017