rs2242116, PTH1R

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.
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 3 46899626 intron variant A/G snv 0.53 0.700 1.000 2 2016 2019