Source: BEFREE

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: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.810 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: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.710 1.000 1 2009 2018
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.050 0.800 5 2011 2017
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma
0.020 1.000 2 2012 2018
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 1.000 1 2014 2014
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0278876
Disease: Adult Medulloblastoma
Adult Medulloblastoma
0.010 1.000 1 2018 2018
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.010 1.000 1 2015 2015
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2014 2014
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0080024
Disease: Piebaldism
Piebaldism
0.010 1.000 1 2015 2015
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
Squamous cell carcinoma of esophagus
0.010 1.000 1 2014 2014
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2011 2011
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0595921
Disease: Intraocular pressure disorder
Intraocular pressure disorder
0.010 1.000 1 2012 2012
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0278510
Disease: Childhood Medulloblastoma
Childhood Medulloblastoma
0.010 1.000 1 2018 2018
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2009 2009
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0025149
Disease: Medulloblastoma
Medulloblastoma
0.010 1.000 1 2018 2018
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2011 2011
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs1063192
rs1063192
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
Malignant neoplasm of urinary bladder
0.010 1.000 1 2014 2014
dbSNP: rs1431316232
rs1431316232
1.000 0.040 9 22006021 missense variant A/G snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 1997 1997
dbSNP: rs1475218156
rs1475218156
1.000 0.080 9 22006096 missense variant C/G;T snv 4.2E-06; 8.4E-06
CUI: C0025286
Disease: Meningioma
Meningioma
0.010 1.000 1 2001 2001
dbSNP: rs1487774219
rs1487774219
1.000 0.040 9 22008910 missense variant T/C snv 8.1E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2006 2006
dbSNP: rs1487774219
rs1487774219
1.000 0.040 9 22008910 missense variant T/C snv 8.1E-06
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2006 2006