rs1010553, STAB1

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.
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 1.000 0.080 3 52506757 synonymous variant T/C snv 0.53 0.59 0.700 1.000 1 2016 2016
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 1.000 0.080 3 52506757 synonymous variant T/C snv 0.53 0.59 0.010 1.000 1 2019 2019