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: rs10089517
rs10089517 		0.925 0.040 8 59266162 intergenic variant C/A snv 0.31
CUI: C0020490
Disease: Hyperopia
Hyperopia 		0.700 1.000 1 2014 2014
dbSNP: rs11073060
rs11073060 		1.000 0.040 15 34697650 intergenic variant C/A snv 0.41
CUI: C0020490
Disease: Hyperopia
Hyperopia 		0.700 1.000 1 2014 2014
dbSNP: rs12193446
rs12193446
LAMA2 ; LOC102723409
0.925 0.040 6 129498893 intron variant A/G snv 6.4E-02
CUI: C0020490
Disease: Hyperopia
Hyperopia 		0.700 1.000 1 2014 2014
dbSNP: rs17648524
rs17648524
RBFOX1
0.882 0.040 16 7409682 intron variant G/C snv 0.29
CUI: C0020490
Disease: Hyperopia
Hyperopia 		0.700 1.000 1 2014 2014
dbSNP: rs2352179
rs2352179
GRID1
1.000 0.040 10 86030323 intron variant C/T snv 0.20
CUI: C0020490
Disease: Hyperopia
Hyperopia 		0.700 1.000 1 2018 2018
dbSNP: rs429358
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0020490
Disease: Hyperopia
Hyperopia 		0.700 1.000 1 2018 2018