rs7818511, GSR

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 8 30719572 intron variant T/C snv 0.76 0.010 1.000 1 2018 2018