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: rs10776482
rs10776482 		4 38773164 synonymous variant A/G snv 0.25 0.23
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10776483
rs10776483 		4 38773419 synonymous variant A/G snv 0.26 0.23
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11096955
rs11096955 		0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11096955
rs11096955 		0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41
CUI: C0025281
Disease: Meniere Disease
Meniere Disease 		Otorhinolaryngologic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11096955
rs11096955 		0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11096955
rs11096955 		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) 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11096955
rs11096955 		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 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11096956
rs11096956 		4 38774559 synonymous variant C/A;T snv 0.25; 4.3E-06
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11096957
rs11096957 		0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0409952
Disease: Idiopathic osteoarthritis
Idiopathic osteoarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11096957
rs11096957 		0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11096957
rs11096957 		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 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11096957
rs11096957 		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 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11096957
rs11096957 		0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2015 2015
dbSNP: rs11096957
rs11096957 		0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C1384584
Disease: Generalized osteoarthritis
Generalized osteoarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11096957
rs11096957 		0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11096957
rs11096957 		0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018