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: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.040 1.000 4 2012 2020
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma
0.020 1.000 2 2008 2019
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.020 1.000 2 2015 2019
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0019158
Disease: Hepatitis
Hepatitis
0.010 1.000 1 2018 2018
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0019159
Disease: Hepatitis A
Hepatitis A
0.010 1.000 1 2018 2018
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0031099
Disease: Periodontitis
Periodontitis
0.010 1.000 1 2019 2019
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.010 1.000 1 2013 2013
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2019 2019
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome
0.010 1.000 1 2012 2012
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.010 1.000 1 2017 2017
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs2149356
rs2149356
0.742 0.360 9 117711921 intron variant T/G snv 0.54
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2015 2015