TLR10, toll like receptor 10, 81793

N. diseases: 71; N. variants: 25
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0018213
Disease: Graves Disease
Graves Disease
Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
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
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
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs10034903
rs10034903
4 38783057 upstream gene variant C/G snv 0.35
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs113143765
rs113143765
4 38783103 upstream gene variant -/A delins
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11466617
rs11466617
1.000 0.040 4 38778850 intron variant T/C snv 0.13
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11466617
rs11466617
1.000 0.040 4 38778850 intron variant T/C snv 0.13
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.010 < 0.001 1 2018 2018
dbSNP: rs11466640
rs11466640
4 38777282 intron variant G/A;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11466645
rs11466645
4 38776582 intron variant A/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11725309
rs11725309
4 38782227 intron variant T/C snv 0.14
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs28393318
rs28393318
1.000 0.080 4 38782646 intron variant A/G snv 0.29
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs28393318
rs28393318
1.000 0.080 4 38782646 intron variant A/G snv 0.29
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4274855
rs4274855
4 38775850 5 prime UTR variant C/T snv 0.13
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs4513579
rs4513579
4 38772195 downstream gene variant T/C snv 0.23
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7653908
rs7653908
4 38780600 intron variant G/C snv 0.22
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7658893
rs7658893
4 38780799 intron variant G/A snv 0.33
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7694115
rs7694115
4 38777473 intron variant A/G snv 0.40
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs866195758
rs866195758
0.925 0.080 4 38774477 frameshift variant GCAGTTGGAT/- del
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs866195758
rs866195758
0.925 0.080 4 38774477 frameshift variant GCAGTTGGAT/- del
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11466657
rs11466657
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
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2016 2016