rs12037987, WNT2B

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.
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 1 112500200 intron variant T/C snv 8.6E-02 0.700 1.000 1 2018 2018
Potassium measurement
CUI: C0202194
Disease: Potassium measurement
28 1 112500200 intron variant T/C snv 8.6E-02 0.700 1.000 1 2018 2018