CD244, CD244 molecule, 51744

N. diseases: 42; N. variants: 6
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: rs4656940
rs4656940
1.000 0.040 1 160860478 intron variant A/G snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.800 1.000 1 2010 2010
dbSNP: rs3766379
rs3766379
0.851 0.320 1 160837925 intron variant T/C snv 0.57
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 0
dbSNP: rs3766377
rs3766377
1.000 0.080 1 160830769 3 prime UTR variant A/G snv 0.34
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs3766379
rs3766379
0.851 0.320 1 160837925 intron variant T/C snv 0.57
CUI: C0027697
Disease: Nephritis
Nephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs3766379
rs3766379
0.851 0.320 1 160837925 intron variant T/C snv 0.57
Neuropsychiatric Systemic Lupus Erythematosus
Infections; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs3766379
rs3766379
0.851 0.320 1 160837925 intron variant T/C snv 0.57
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs4656942
rs4656942
0.851 0.160 1 160861258 intron variant G/A;C;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.010 1.000 1 2015 2015
dbSNP: rs4656942
rs4656942
0.851 0.160 1 160861258 intron variant G/A;C;T snv
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs4656942
rs4656942
0.851 0.160 1 160861258 intron variant G/A;C;T snv
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs4656942
rs4656942
0.851 0.160 1 160861258 intron variant G/A;C;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs485618
rs485618
0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs485618
rs485618
0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs485618
rs485618
0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.010 1.000 1 2015 2015
dbSNP: rs485618
rs485618
0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs6682654
rs6682654
0.882 0.320 1 160839213 intron variant G/A snv 0.45
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs6682654
rs6682654
0.882 0.320 1 160839213 intron variant G/A snv 0.45
Neuropsychiatric Systemic Lupus Erythematosus
Infections; Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs6682654
rs6682654
0.882 0.320 1 160839213 intron variant G/A snv 0.45
CUI: C0027697
Disease: Nephritis
Nephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2010 2010