rs7541039, PROX1

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 1 214003436 intron variant C/T snv 0.27 0.700 1.000 1 2019 2019
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 1 214003436 intron variant C/T snv 0.27 0.700 1.000 1 2016 2016