rs926103, SH2D2A;NTRK1

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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.925 0.120 1 156815190 missense variant T/C snv 0.64 0.57 0.700 1.000 1 2019 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.925 0.120 1 156815190 missense variant T/C snv 0.64 0.57 0.010 1.000 1 2008 2008