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: rs1000113
rs1000113
IRGM
0.925 0.040 5 150860514 intron variant C/T snv 0.13
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2009 2009
dbSNP: rs10001410
rs10001410
ADGRL3
1.000 0.040 4 61608511 intron variant C/A snv 0.55
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.010 1.000 1 2019 2019
dbSNP: rs1000256867
rs1000256867
TP53
17 7673550 missense variant T/A;G snv 4.0E-06
CUI: C0333875
Disease: High-Grade Squamous Intraepithelial Lesions
High-Grade Squamous Intraepithelial Lesions 		0.010 1.000 1 2020 2020
dbSNP: rs1000283
rs1000283
HSD11B1 ; HSD11B1-AS1
0.925 0.080 1 209721316 intron variant G/A snv 0.18
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2011 2011
dbSNP: rs1000283
rs1000283
HSD11B1 ; HSD11B1-AS1
0.925 0.080 1 209721316 intron variant G/A snv 0.18
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2011 2011
dbSNP: rs10004195
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.010 1.000 1 2019 2019
dbSNP: rs10004195
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
Autoimmune thyroid disease (AITD) 		0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		0.010 1.000 1 2011 2011
dbSNP: rs10004195
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies 		0.010 1.000 1 2015 2015
dbSNP: rs1000592
rs1000592 		1.000 0.040 2 118939624 upstream gene variant C/A snv 6.4E-03
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder 		0.010 1.000 1 2014 2014
dbSNP: rs1000731
rs1000731
DISC1 ; TSNAX-DISC1 ; LOC105373170
1.000 0.040 1 231827745 intron variant C/T snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 < 0.001 1 2018 2018
dbSNP: rs1000778
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2017 2017
dbSNP: rs10008257
rs10008257 		0.925 0.040 4 94435177 intergenic variant G/A snv 0.63
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2008 2008
dbSNP: rs10008492
rs10008492 		1.000 0.120 4 38764099 intergenic variant C/G;T snv
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2009 2009
dbSNP: rs10009145
rs10009145
ADH4 ; LOC100507053
1.000 0.080 4 99126778 intron variant G/A snv 0.39 0.34
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.010 1.000 1 2012 2012
dbSNP: rs10009228
rs10009228
CHRNA9
4 40354405 missense variant A/G snv 0.78 0.76
CUI: C0178874
Disease: Tumor Progression
Tumor Progression 		0.010 1.000 1 2012 2012
dbSNP: rs1000952
rs1000952
HTR3D
1.000 0.040 3 184038034 missense variant G/A;C;T snv 0.66; 3.6E-05; 4.0E-06
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder 		0.010 1.000 1 2014 2014
dbSNP: rs10010131
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2008 2008
dbSNP: rs10010131
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.010 1.000 1 2008 2008
dbSNP: rs10010131
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2008 2008
dbSNP: rs10010131
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2008 2008
dbSNP: rs10010131
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2008 2008