rs7780752, GNGT1

N. diseases: 2
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.
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 7 93612328 intron variant T/C snv 0.27 0.800 1.000 1 2013 2013
Body mass index
CUI: C1305855
Disease: Body mass index
2689 7 93612328 intron variant T/C snv 0.27 0.700 1.000 1 2017 2017