Source: GWASDB

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: rs4656461
rs4656461
0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.810 1.000 1 2011 2012
dbSNP: rs523096
rs523096
0.827 0.080 9 22019130 intron variant A/G snv 0.30
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.810 1.000 1 2012 2012
dbSNP: rs3213787
rs3213787
0.925 0.040 2 45419685 intron variant A/G snv 4.3E-02
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.800 1.000 1 2010 2010
dbSNP: rs4977756
rs4977756
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.800 1.000 1 2011 2011
dbSNP: rs2165241
rs2165241
0.716 0.360 15 73929861 intron variant T/C snv 0.60
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.750 1.000 1 2007 2019
dbSNP: rs1048661
rs1048661
0.732 0.320 15 73927205 missense variant G/T snv 0.33 0.28
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.730 1.000 1 2007 2017
dbSNP: rs10120688
rs10120688
0.807 0.080 9 22056500 intron variant G/A snv 0.50
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.710 1.000 1 2012 2012
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.710 1.000 1 2011 2017
dbSNP: rs10152898
rs10152898
1.000 0.040 15 73962780 intergenic variant G/A;T snv
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2007 2007
dbSNP: rs10965219
rs10965219
0.882 0.080 9 22053688 intron variant A/G snv 0.58
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2012 2012
dbSNP: rs12440667
rs12440667
1.000 0.040 15 73939098 intron variant C/A;T snv
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2007 2007
dbSNP: rs1412829
rs1412829
0.742 0.400 9 22043927 intron variant A/G snv 0.28
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2011 2011
dbSNP: rs1992314
rs1992314
0.925 0.040 15 73931426 intron variant C/G snv 0.29
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2007 2007
dbSNP: rs2028386
rs2028386
1.000 0.040 15 73934367 intron variant C/A;G snv
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2007 2007
dbSNP: rs2304719
rs2304719
1.000 0.040 15 73943159 intron variant C/T snv 0.30
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2007 2007
dbSNP: rs3217992
rs3217992
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2012 2012
dbSNP: rs4243042
rs4243042
1.000 0.040 15 73949283 intron variant A/T snv 0.37
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2007 2007
dbSNP: rs4337252
rs4337252
1.000 0.040 15 73934424 intron variant G/C snv 0.52
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2007 2007
dbSNP: rs4886782
rs4886782
1.000 0.040 15 73936469 intron variant G/A snv 0.27
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2007 2007
dbSNP: rs504022
rs504022
1.000 0.040 21 43311258 regulatory region variant T/G snv 0.91
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2011 2011
dbSNP: rs518394
rs518394
0.827 0.160 9 22019674 intron variant G/C snv 0.30
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2012 2012
dbSNP: rs564398
rs564398
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2012 2012
dbSNP: rs643319
rs643319
0.882 0.080 9 22017837 intron variant C/A snv 0.40
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2012 2012
dbSNP: rs7034696
rs7034696
1.000 0.040 9 18804132 intron variant C/T snv 0.27
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2011 2011
dbSNP: rs7049105
rs7049105
0.807 0.120 9 22028802 intron variant A/G snv 0.58
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2011 2011