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: rs1330189219
rs1330189219
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2008 2008
dbSNP: rs1330189219
rs1330189219
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2008 2008
dbSNP: rs1330189219
rs1330189219
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2008 2008
dbSNP: rs1330189219
rs1330189219
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2008 2008
dbSNP: rs1330189219
rs1330189219
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2008 2008
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 1.000 1 2015 2015
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0003467
Disease: Anxiety
Anxiety
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C2747816
Disease: Complicated malaria
Complicated malaria
0.010 1.000 1 2007 2007
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C4552332
Disease: Congenital Zika syndrome
Congenital Zika syndrome
0.010 1.000 1 2019 2019
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer
0.010 1.000 1 2014 2014
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.010 1.000 1 2017 2017
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0040561
Disease: Ocular Toxoplasmosis
Ocular Toxoplasmosis
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2018 2018
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
Immune Reconstitution Inflammatory Syndrome
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 1.000 1 2020 2020
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0030193
Disease: Pain
Pain
0.010 1.000 1 2012 2012
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1096197
Disease: Immune reconstitution syndrome
Immune reconstitution syndrome
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism
0.010 1.000 1 2013 2013