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: rs9461776
rs9461776
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.010 1.000 1 2017 2017
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
0.010 1.000 1 2016 2016
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2016 2016
dbSNP: rs17879469
rs17879469
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05
CUI: C0178468
Disease: Autoimmune thyroid disease
Autoimmune thyroid disease
0.010 1.000 1 2003 2003
dbSNP: rs9461776
rs9461776
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02
CUI: C0746351
Disease: Benign Lymphoproliferative Disorder
Benign Lymphoproliferative Disorder
0.010 1.000 1 2017 2017
dbSNP: rs9461776
rs9461776
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma
0.010 1.000 1 2017 2017
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 1.000 1 2013 2016
dbSNP: rs17879469
rs17879469
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05
Diabetes Mellitus, Insulin-Dependent
0.030 1.000 3 1998 2003
dbSNP: rs2858870
rs2858870
0.851 0.280 6 32604474 intergenic variant T/A;C snv
CUI: C0014038
Disease: Encephalitis
Encephalitis
0.010 1.000 1 2018 2018
dbSNP: rs1136758
rs1136758
1.000 0.080 6 32584355 missense variant T/A;C;G snv 0.25; 2.7E-02; 4.7E-05; 1.6E-05; 7.6E-03
CUI: C0014070
Disease: Encephalomyelitis
Encephalomyelitis
0.010 1.000 1 2004 2004
dbSNP: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.010 1.000 1 2011 2011
dbSNP: rs17879469
rs17879469
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.020 0.500 2 2003 2005
dbSNP: rs17879469
rs17879469
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
0.010 1.000 1 2001 2001
dbSNP: rs17879702
rs17879702
1.000 0.080 6 32584346 missense variant G/A snv 3.2E-02 5.7E-02
CUI: C0019158
Disease: Hepatitis
Hepatitis
0.010 1.000 1 2016 2016
dbSNP: rs17879702
rs17879702
1.000 0.080 6 32584346 missense variant G/A snv 3.2E-02 5.7E-02
CUI: C0019159
Disease: Hepatitis A
Hepatitis A
0.010 1.000 1 2016 2016
dbSNP: rs477515
rs477515
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 1.000 1 2014 2014
dbSNP: rs9461776
rs9461776
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 1.000 1 2017 2017
dbSNP: rs2308765
rs2308765
6 32581757 missense variant A/C;G;T snv 7.6E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2012 2012
dbSNP: rs17879469
rs17879469
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism
0.010 1.000 1 2012 2012
dbSNP: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
Idiopathic Membranous Glomerulonephritis
0.010 1.000 1 2017 2017
dbSNP: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.810 1.000 1 2011 2015
dbSNP: rs9271117
rs9271117
0.925 0.160 6 32609018 intergenic variant C/T snv 0.72
CUI: C0021400
Disease: Influenza
Influenza
0.010 1.000 1 2013 2013
dbSNP: rs2647073
rs2647073
1.000 0.080 6 32606237 intergenic variant A/C snv 0.12
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs16822805
rs16822805
1.000 0.080 6 32584172 missense variant C/A;G;T snv 6.1E-04; 7.6E-03
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2000 2000
dbSNP: rs17886882
rs17886882
1.000 0.080 6 32584171 missense variant G/A;C;T snv 9.0E-04; 0.12
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2000 2000