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: rs9913911
rs9913911
0.925 0.040 17 10127866 intron variant A/G snv 0.32
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 6 2014 2018
dbSNP: rs2745572
rs2745572
0.925 0.040 6 1548134 intergenic variant A/G snv 0.31
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 4 2017 2018
dbSNP: rs9853115
rs9853115
0.925 0.040 3 186413811 intergenic variant T/A;G snv 0.51
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 4 2017 2018
dbSNP: rs10036789
rs10036789
1.000 0.080 5 72400091 regulatory region variant C/A;G snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs10281637
rs10281637
1.000 0.040 7 116511284 downstream gene variant T/C snv 0.28
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2017 2018
dbSNP: rs10918274
rs10918274
1.000 0.040 1 165745179 intron variant T/C snv 0.89
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2017 2018
dbSNP: rs11217878
rs11217878
1.000 0.040 11 120469674 intron variant G/A snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2015 2018
dbSNP: rs113542380
rs113542380
2 43237679 intron variant G/A snv 4.7E-02
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs113985657
rs113985657
1.000 0.040 6 597203 intron variant C/T snv 0.14
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs1579050
rs1579050
0.925 0.040 2 152508013 intron variant A/G snv 0.42
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs163524
rs163524
2 44930414 intron variant C/A snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs2472493
rs2472493
0.851 0.040 9 104933567 downstream gene variant G/A snv 0.61
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2014 2018
dbSNP: rs327716
rs327716
7 81209661 regulatory region variant A/G;T snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs3743860
rs3743860
16 89752083 intron variant T/C snv 0.47
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs3791979
rs3791979
1.000 0.040 2 217802649 3 prime UTR variant T/A;C;G snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs4141194
rs4141194
11 16989629 intron variant C/A snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs4672075
rs4672075
2 55816667 intergenic variant C/G snv 0.55
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs4775427
rs4775427
15 61659036 intron variant C/T snv 0.42
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs6065171
rs6065171
20 39910126 regulatory region variant T/C;G snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs6732795
rs6732795
2 69184385 intron variant A/C snv 0.51
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2017 2018
dbSNP: rs7555523
rs7555523
0.925 0.040 1 165749742 intron variant C/A snv 0.88
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2012 2017
dbSNP: rs76020419
rs76020419
8 6502768 3 prime UTR variant G/T snv 2.7E-02
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs7635832
rs7635832
3 172271486 intron variant T/G snv 0.22
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2017 2018
dbSNP: rs7924522
rs7924522
1.000 0.040 11 128510847 intron variant C/A snv 0.70
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs9494457
rs9494457
1.000 0.040 6 136153656 intron variant T/A snv 0.39
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018