rs13322435, None

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.
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 3 157077679 upstream gene variant A/G snv 0.46 0.700 1.000 2 2016 2019
Age at menarche
CUI: C1314691
Disease: Age at menarche
591 3 157077679 upstream gene variant A/G snv 0.46 0.700 1.000 1 2019 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 3 157077679 upstream gene variant A/G snv 0.46 0.700 1.000 1 2019 2019