rs6598008, CDHR5

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.
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.925 0.080 11 618172 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
96 0.925 0.080 11 618172 intron variant A/G snv 0.48 0.010 1.000 1 2017 2017