rs7903146, TCF7L2

N. diseases: 93
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 0.554 0.680 10 112998590 intron variant C/G;T snv 0.700 1.000 1 2019 2019