rs1039659576, MTR

N. diseases: 21
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.
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
45 0.689 0.520 1 236803473 missense variant A/G snv 0.010 1.000 1 2018 2018