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: rs1711745
rs1711745
INIP
0.925 0.120 9 112690629 intron variant C/A snv 0.13
CUI: C0454651
Disease: Specific language impairment
Specific language impairment 		0.700 1.000 1 2014 2014
dbSNP: rs1711745
rs1711745
INIP
0.925 0.120 9 112690629 intron variant C/A snv 0.13
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2014 2014
dbSNP: rs1711745
rs1711745
INIP
0.925 0.120 9 112690629 intron variant C/A snv 0.13
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.700 1.000 1 2014 2014