CCR6, C-C motif chemokine receptor 6, 1235

N. diseases: 231; N. variants: 13
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: rs3093024
rs3093024 		0.882 0.200 6 167119305 non coding transcript exon variant A/G snv 0.61
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.810 1.000 2 2010 2014
dbSNP: rs1571878
rs1571878 		1.000 0.120 6 167127354 intron variant C/T snv 0.61
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 4 2012 2019
dbSNP: rs3093023
rs3093023 		0.851 0.160 6 167120802 intron variant G/A snv 0.34
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 3 2010 2014
dbSNP: rs1854853
rs1854853 		1.000 0.120 6 167119574 intron variant A/G snv 0.48
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 1 2014 2014
dbSNP: rs59466457
rs59466457 		1.000 0.120 6 167124266 intron variant A/G snv 1.6E-03
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs1556413
rs1556413 		1.000 0.120 6 167111255 intron variant G/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs1855025
rs1855025 		1.000 0.120 6 167124106 intron variant A/G snv 0.40
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs2023305
rs2023305 		0.851 0.280 6 167111410 intron variant C/T snv 0.38
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs3093009
rs3093009 		1.000 0.080 6 167135989 intron variant A/G snv 0.30
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs3093023
rs3093023 		0.851 0.160 6 167120802 intron variant G/A snv 0.34
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3093023
rs3093023 		0.851 0.160 6 167120802 intron variant G/A snv 0.34
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3093023
rs3093023 		0.851 0.160 6 167120802 intron variant G/A snv 0.34
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs62436827
rs62436827 		6 167135059 non coding transcript exon variant A/G snv 7.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2014 2014
dbSNP: rs10946216
rs10946216 		1.000 0.040 6 167125409 intron variant T/C snv 0.61
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2023305
rs2023305 		0.851 0.280 6 167111410 intron variant C/T snv 0.38
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2023305
rs2023305 		0.851 0.280 6 167111410 intron variant C/T snv 0.38
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2023305
rs2023305 		0.851 0.280 6 167111410 intron variant C/T snv 0.38
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3093023
rs3093023 		0.851 0.160 6 167120802 intron variant G/A snv 0.34
CUI: C1262313
Disease: Invasive Fungal Infections
Invasive Fungal Infections 		Infections 0.010 < 0.001 1 2011 2011
dbSNP: rs3093023
rs3093023 		0.851 0.160 6 167120802 intron variant G/A snv 0.34
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3093023
rs3093023 		0.851 0.160 6 167120802 intron variant G/A snv 0.34
CUI: C0867389
Disease: Chronic graft-versus-host disease
Chronic graft-versus-host disease 		Immune System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3093024
rs3093024 		0.882 0.200 6 167119305 non coding transcript exon variant A/G snv 0.61
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3093024
rs3093024 		0.882 0.200 6 167119305 non coding transcript exon variant A/G snv 0.61
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs555016384
rs555016384 		6 167136139 missense variant G/A snv 4.0E-06 7.0E-06
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2010 2010
dbSNP: rs748148861
rs748148861 		0.925 0.120 6 167136856 missense variant G/C snv 8.0E-06
CUI: C0007107
Disease: Malignant neoplasm of larynx
Malignant neoplasm of larynx 		Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs748148861
rs748148861 		0.925 0.120 6 167136856 missense variant G/C snv 8.0E-06
CUI: C0595989
Disease: Carcinoma of larynx
Carcinoma of larynx 		Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014