rs3917862, SELP

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.
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 1.000 0.040 1 169623875 intron variant A/G snv 3.9E-02 0.010 1.000 1 2019 2019
Violence
CUI: C0042693
Disease: Violence
6 1.000 0.040 1 169623875 intron variant A/G snv 3.9E-02 0.010 1 2019 2019