rs1818782, DAB2;C9

N. diseases: 3
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.
Aspartate aminotransferase measurement
76 5 39424526 intron variant A/C snv 0.56 0.700 1.000 1 2018 2018
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 5 39424526 intron variant A/C snv 0.56 0.700 1.000 1 2019 2019
Body Height
CUI: C0005890
Disease: Body Height
3972 5 39424526 intron variant A/C snv 0.56 0.700 1.000 1 2019 2019