PCGF3, polycomb group ring finger 3, 10336

N. diseases: 8; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs142708984
rs142708984
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
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
4 735866 intron variant A/T snv 6.4E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018