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: rs2010963
rs2010963
0.630 0.607 6 43770613 5 prime UTR variant C/G snp 0.70
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)
0.700 1 2002 2002
dbSNP: rs833070
rs833070
0.923 0.179 6 43774889 non coding transcript exon variant T/C snp 0.57
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1 2017 2017
dbSNP: rs833070
rs833070
0.923 0.179 6 43774889 non coding transcript exon variant T/C snp 0.57
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1 2017 2017
dbSNP: rs833070
rs833070
0.923 0.179 6 43774889 non coding transcript exon variant T/C snp 0.57
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1 2017 2017
dbSNP: rs2010963
rs2010963
0.630 0.607 6 43770613 5 prime UTR variant C/G snp 0.70
CUI: C0017638
Disease: Glioma
Glioma
0.020 1.000 2 2010 2016
dbSNP: rs25648
rs25648
0.769 0.357 6 43771240 synonymous variant C/G,T snp 8.5E-06; 0.16 0.14
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2007 2015
dbSNP: rs25648
rs25648
0.769 0.357 6 43771240 synonymous variant C/G,T snp 8.5E-06; 0.16 0.14
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2007 2015
dbSNP: rs3025039
rs3025039
0.638 0.536 6 43784799 3 prime UTR variant C/T snp 0.13
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.020 1.000 2 2011 2012
dbSNP: rs3025039
rs3025039
0.638 0.536 6 43784799 3 prime UTR variant C/T snp 0.13
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2010 2012
dbSNP: rs3025039
rs3025039
0.638 0.536 6 43784799 3 prime UTR variant C/T snp 0.13
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome
0.020 1.000 2 2006 2012
dbSNP: rs3025039
rs3025039
0.638 0.536 6 43784799 3 prime UTR variant C/T snp 0.13
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2010 2012
dbSNP: rs699947
rs699947
0.667 0.571 6 43768652 intergenic variant A/C,T snp 0.59
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
0.020 1.000 2 2007 2010
dbSNP: rs752907384
rs752907384
0.846 0.107 6 43782077 missense variant C/G,T snp 8.0E-06
CUI: C0032461
Disease: Polycythemia
Polycythemia
0.020 1.000 2 2004 2006
dbSNP: rs10434
rs10434
0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434
0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59
CUI: C0041582
Disease: Ulcer
Ulcer
0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434
0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59
CUI: C0038358
Disease: Gastric ulcer
Gastric ulcer
0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434
0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.010 1.000 1 2015 2015
dbSNP: rs10434
rs10434
0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.010 1.000 1 2015 2015
dbSNP: rs10434
rs10434
0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59
CUI: C0013295
Disease: Duodenal Ulcer
Duodenal Ulcer
0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434
0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2009 2009
dbSNP: rs10434
rs10434
0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.010 1.000 1 2009 2009
dbSNP: rs13207351
rs13207351
1.000 0.143 6 43770057 regulatory region variant A/G,T snp 0.57
CUI: C0154830
Disease: Proliferative diabetic retinopathy
Proliferative diabetic retinopathy
0.010 1.000 1 2008 2008
dbSNP: rs140461341
rs140461341
6 43782078 missense variant G/A snp 3.6E-05
CUI: C1519680
Disease: Tumor Immunity
Tumor Immunity
0.010 1.000 1 2018 2018
dbSNP: rs141138308
rs141138308
1.000 0.036 6 43780784 missense variant C/A,T snp 4.0E-06; 2.8E-05 3.2E-05
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.010 1.000 1 2006 2006
dbSNP: rs1413711
rs1413711
1.000 0.107 6 43772941 intron variant T/A,C snp 0.57
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
0.010 1.000 1 2011 2011