rs12889267, ARHGEF40

N. diseases: 4
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 14 21074607 missense variant A/G snv 0.16 0.13 0.700 1.000 1 2016 2016
Lean body mass
CUI: C0424678
Disease: Lean body mass
211 14 21074607 missense variant A/G snv 0.16 0.13 0.700 1.000 1 2019 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 14 21074607 missense variant A/G snv 0.16 0.13 0.700 1.000 1 2019 2019
RESTING HEART RATE
CUI: C1821417
Disease: RESTING HEART RATE
134 14 21074607 missense variant A/G snv 0.16 0.13 0.700 1.000 1 2016 2016