CD247, CD247 molecule, 919

N. diseases: 140; 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: rs2056626
rs2056626 		0.882 0.080 1 167451188 intron variant T/G snv 0.30
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.830 1.000 5 2010 2019
dbSNP: rs2056626
rs2056626 		0.882 0.080 1 167451188 intron variant T/G snv 0.30
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.710 1.000 2 2011 2013
dbSNP: rs7523907
rs7523907 		1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2019 2019
dbSNP: rs864537
rs864537 		0.925 0.200 1 167442147 intron variant A/G snv 0.29
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.810 1.000 2 2011 2013
dbSNP: rs1052231
rs1052231 		1.000 0.080 1 167430837 3 prime UTR variant T/A snv 0.82
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10918706
rs10918706 		0.925 0.200 1 167496884 intron variant C/T snv 0.24
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2012 2012
dbSNP: rs10918706
rs10918706 		0.925 0.200 1 167496884 intron variant C/T snv 0.24
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12133337
rs12133337 		0.925 0.160 1 167483453 intron variant T/C snv 0.17
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2012 2012
dbSNP: rs12133337
rs12133337 		0.925 0.160 1 167483453 intron variant T/C snv 0.17
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1214598
rs1214598 		0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1214598
rs1214598 		0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1214598
rs1214598 		0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1214611
rs1214611 		0.925 0.200 1 167479867 intron variant A/G snv 0.54
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1214611
rs1214611 		0.925 0.200 1 167479867 intron variant A/G snv 0.54
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs1617333
rs1617333 		0.925 0.080 1 167467033 intron variant A/G snv 0.27
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1617333
rs1617333 		0.925 0.080 1 167467033 intron variant A/G snv 0.27
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1723018
rs1723018 		1.000 0.080 1 167464183 intron variant A/G snv 0.33
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1723022
rs1723022 		1.000 0.040 1 167436181 intron variant G/T snv 0.25
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2056625
rs2056625 		0.925 0.080 1 167451062 intron variant G/A snv 0.27
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2056625
rs2056625 		0.925 0.080 1 167451062 intron variant G/A snv 0.27
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 1 2019 2019
dbSNP: rs2056626
rs2056626 		0.882 0.080 1 167451188 intron variant T/G snv 0.30
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2056626
rs2056626 		0.882 0.080 1 167451188 intron variant T/G snv 0.30
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease 		Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2056626
rs2056626 		0.882 0.080 1 167451188 intron variant T/G snv 0.30
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 1 2019 2019
dbSNP: rs2949655
rs2949655 		1.000 0.120 1 167482613 intron variant G/A snv 0.39
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2949661
rs2949661 		1 167455687 intron variant C/A;G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019