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: rs10774547
rs10774547 		0.925 0.120 12 120424913 intergenic variant T/C snv 0.39
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.700 1.000 1 2014 2014
dbSNP: rs11855415
rs11855415
PCSK6 ; PCSK6-AS1
1.000 0.120 15 101334918 intron variant A/T snv 0.80
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.700 1.000 1 2011 2011
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
dbSNP: rs59197085
rs59197085
CCDC136
0.925 0.120 7 128820702 intron variant G/A snv 9.9E-02
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.700 1.000 1 2014 2014
dbSNP: rs5995177
rs5995177
RBFOX2
0.925 0.120 22 35913505 intron variant G/A;C snv
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.700 1.000 1 2014 2014
dbSNP: rs7182874
rs7182874
PCSK6
1.000 0.120 15 101325267 intron variant T/C snv 0.71
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.700 1.000 1 2013 2013