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: rs56011263
rs56011263
PCGF3
4 709183 intron variant T/C snv 0.35
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs11734460
rs11734460
PCGF3
4 711285 intron variant C/A;T snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs11734460
rs11734460
PCGF3
4 711285 intron variant C/A;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs11734460
rs11734460
PCGF3
4 711285 intron variant C/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs11734460
rs11734460
PCGF3
4 711285 intron variant C/A;T snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs142708984
rs142708984
PCGF3
4 707538 intron variant C/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs75751670
rs75751670
PCGF3
4 707252 intron variant G/A snv 0.10
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs79713586
rs79713586
PCGF3
4 735866 intron variant A/T snv 6.4E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs79839061
rs79839061
PCGF3
4 712095 intron variant G/A snv 9.6E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019