Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12889267
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs12889267
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2016 2016
dbSNP: rs12889267
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs12889267
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs8019890
rs8019890
ARHGEF40 ; NDRG2
14 21069908 intron variant C/A snv 0.45
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019