Source: ALL

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: 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: rs12471183
rs12471183
2 152510313 intron variant T/C snv 0.39
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs1579050
rs1579050
0.925 0.040 2 152508013 intron variant A/G snv 0.42
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2018 2018
dbSNP: rs1579050
rs1579050
0.925 0.040 2 152508013 intron variant A/G snv 0.42
CUI: C0339682
Disease: Regular astigmatism - corneal
Regular astigmatism - corneal
0.700 1.000 1 2018 2018
dbSNP: rs2304556
rs2304556
2 152617280 intron variant T/G snv 0.36
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1.000 1 2011 2011
dbSNP: rs34968716
rs34968716
2 152438409 intron variant G/A;C;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs55692468
rs55692468
2 152504861 intron variant T/A;G snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2017 2017
dbSNP: rs6434068
rs6434068
0.925 0.040 2 152501027 intron variant G/C snv 0.41
CUI: C0339682
Disease: Regular astigmatism - corneal
Regular astigmatism - corneal
0.700 1.000 1 2018 2018
dbSNP: rs6434068
rs6434068
0.925 0.040 2 152501027 intron variant G/C snv 0.41
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2018 2018
dbSNP: rs6734194
rs6734194
1.000 0.040 2 152610177 intron variant T/G snv 0.53
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs6741131
rs6741131
1.000 0.040 2 152610088 intron variant G/A snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017