rs10142635, EGLN3

N. diseases: 1
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.
heart rate
CUI: C0018810
Disease: heart rate
103 14 34423401 intron variant A/G snv 3.2E-02 0.700 1.000 1 2018 2018