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: 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: 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: rs35445101
rs35445101
0.925 0.080 6 32579102 missense variant A/G snv 4.2E-04 2.7E-02
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
0.010 1.000 1 2017 2017
dbSNP: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.810 1.000 1 2007 2018
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: C0030567
Disease: Parkinson Disease
Parkinson Disease
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: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2011 2011
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: 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: rs9461776
rs9461776
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
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: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
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: C0543697
Disease: Mixed cryoglobulinemia
Mixed cryoglobulinemia
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: 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: C0024299
Disease: Lymphoma
Lymphoma
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: C0019196
Disease: Hepatitis C
Hepatitis C
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: rs1136759
rs1136759
0.882 0.080 6 32584354 missense variant C/A;G;T snv 8.9E-03; 0.23; 1.2E-04
Steroid resistant nephrotic syndrome of childhood
0.010 1.000 1 2018 2018
dbSNP: rs1136759
rs1136759
0.882 0.080 6 32584354 missense variant C/A;G;T snv 8.9E-03; 0.23; 1.2E-04
Steroid-resistant nephrotic syndrome
0.010 1.000 1 2018 2018
dbSNP: rs1136759
rs1136759
0.882 0.080 6 32584354 missense variant C/A;G;T snv 8.9E-03; 0.23; 1.2E-04
Steroid-sensitive nephrotic syndrome
0.010 1.000 1 2018 2018
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: rs771131230
rs771131230
0.925 0.120 6 32581827 missense variant C/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2011 2011
dbSNP: rs771131230
rs771131230
0.925 0.120 6 32581827 missense variant C/A;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2011 2011
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: 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