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: rs4129009
rs4129009
TLR10
0.882 0.120 4 38773268 missense variant T/A;C;G snv 0.17 0.13
CUI: C0004096
Disease: Asthma
Asthma 		0.020 1.000 2 2017 2018
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: rs11096955
rs11096955
TLR10
0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41
CUI: C0025281
Disease: Meniere Disease
Meniere Disease 		0.010 1.000 1 2013 2013
dbSNP: rs11096955
rs11096955
TLR10
0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs11096955
rs11096955
TLR10
0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2008 2008
dbSNP: rs11096955
rs11096955
TLR10
0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.010 1.000 1 2013 2013
dbSNP: rs11096957
rs11096957
TLR10
0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		0.010 1.000 1 2018 2018
dbSNP: rs11096957
rs11096957
TLR10
0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0263746
Disease: Osteoarthritis of the hand
Osteoarthritis of the hand 		0.010 1.000 1 2018 2018
dbSNP: rs11096957
rs11096957
TLR10
0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C1384584
Disease: Generalized osteoarthritis
Generalized osteoarthritis 		0.010 1.000 1 2018 2018
dbSNP: rs11096957
rs11096957
TLR10
0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0409952
Disease: Idiopathic osteoarthritis
Idiopathic osteoarthritis 		0.010 1.000 1 2018 2018
dbSNP: rs11096957
rs11096957
TLR10
0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2008 2008
dbSNP: rs11096957
rs11096957
TLR10
0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs11096957
rs11096957
TLR10
0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.010 1.000 1 2015 2015
dbSNP: rs11466617
rs11466617
TLR10
1.000 0.040 4 38778850 intron variant T/C snv 0.13
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.010 < 0.001 1 2018 2018
dbSNP: rs11466651
rs11466651
TLR10
0.925 0.120 4 38774699 missense variant C/T snv 6.5E-02 4.6E-02
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.010 1.000 1 2010 2010
dbSNP: rs11466651
rs11466651
TLR10
0.925 0.120 4 38774699 missense variant C/T snv 6.5E-02 4.6E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2010 2010
dbSNP: rs11466653
rs11466653
TLR10
1.000 0.080 4 38774614 missense variant A/G snv 6.4E-02 4.1E-02
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs11466653
rs11466653
TLR10
1.000 0.080 4 38774614 missense variant A/G snv 6.4E-02 4.1E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2013 2013
dbSNP: rs11466657
rs11466657
TLR10
0.925 0.120 4 38774173 missense variant A/G snv 2.7E-02; 4.0E-06 2.4E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2016 2016