rs6556883, RHOBTB3;GLRX

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.
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
45 1.000 5 95816381 intron variant A/G snv 0.78 0.010 1.000 1 2020 2020