LIG4, DNA ligase 4, 3981

N. diseases: 293; N. variants: 24
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: rs375554612
rs375554612
1.000 0.160 13 108209365 frameshift variant T/- delins 3.7E-04
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 4 2001 2016
dbSNP: rs10131
rs10131
1.000 0.040 13 108207498 3 prime UTR variant C/T snv 0.12
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.020 1.000 2 2015 2016
dbSNP: rs104894420
rs104894420
1.000 0.160 13 108209863 missense variant C/T snv
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Immune System Diseases 0.810 1.000 2 2001 2004
dbSNP: rs10131
rs10131
1.000 0.040 13 108207498 3 prime UTR variant C/T snv 0.12
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs10131
rs10131
1.000 0.040 13 108207498 3 prime UTR variant C/T snv 0.12
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs1332784619
rs1332784619
1.000 0.160 13 108210406 missense variant T/C snv 7.0E-06
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1566366148
rs1566366148
1.000 0.160 13 108210469 frameshift variant CT/- delins
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs3093739
rs3093739
1.000 0.040 13 108215053 intron variant A/G snv 8.8E-02
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs759838407
rs759838407
0.925 0.160 13 108209756 frameshift variant AG/-;AGAG delins
CUI: C0013336
Disease: Dwarfism
Dwarfism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs759838407
rs759838407
0.925 0.160 13 108209756 frameshift variant AG/-;AGAG delins
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
Hemic and Lymphatic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs759838407
rs759838407
0.925 0.160 13 108209756 frameshift variant AG/-;AGAG delins
CUI: C0342573
Disease: PITUITARY DWARFISM I
PITUITARY DWARFISM I
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs886037777
rs886037777
1.000 0.160 13 108209957 missense variant A/G snv 7.0E-06
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1060499662
rs1060499662
1.000 0.160 13 108208948 missense variant A/G snv
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Immune System Diseases 0.700 0
dbSNP: rs587776663
rs587776663
1.000 0.160 13 108209969 inframe deletion GTT/- delins
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Immune System Diseases 0.700 0
dbSNP: rs751070095
rs751070095
1.000 0.160 13 108210386 frameshift variant ATTTC/- delins
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Immune System Diseases 0.700 0
dbSNP: rs751409106
rs751409106
1.000 0.080 13 108209596 missense variant T/C;G snv 4.0E-06
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.700 0
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.030 1.000 3 2002 2014
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.030 1.000 3 2002 2014
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2004 2012
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2004 2012
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2004 2012
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
CUI: C0030319
Disease: Panic Disorder
Panic Disorder
Mental Disorders 0.010 < 0.001 1 2015 2015
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1326656542
rs1326656542
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2012 2012