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: rs9388490
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs9388490
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs9388490
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs9388490
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017