RECQL4, RecQ like helicase 4, 9401

N. diseases: 249; N. variants: 73
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: rs2721173
rs2721173 		8 144519045 intron variant C/T snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 3 2017 2019
dbSNP: rs1286406860
rs1286406860 		8 144513128 missense variant A/G snv 4.9E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2004 2004
dbSNP: rs3757966
rs3757966 		8 144519234 intron variant G/A snv 0.38
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs3757966
rs3757966 		8 144519234 intron variant G/A snv 0.38
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs4244612
rs4244612 		8 144516318 missense variant C/G snv 0.44 0.42
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs557142414
rs557142414 		8 144515395 missense variant G/A snv 1.6E-04 4.2E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2004 2004
dbSNP: rs386833845
rs386833845 		0.827 0.240 8 144514983 frameshift variant A/- del 2.4E-04 3.3E-04
CUI: C2698314
Disease: B lymphoblastic leukemia lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)
B lymphoblastic leukemia lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1) 		0.700 0
dbSNP: rs386833845
rs386833845 		0.827 0.240 8 144514983 frameshift variant A/- del 2.4E-04 3.3E-04
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 0
dbSNP: rs386833845
rs386833845 		0.827 0.240 8 144514983 frameshift variant A/- del 2.4E-04 3.3E-04
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs386833845
rs386833845 		0.827 0.240 8 144514983 frameshift variant A/- del 2.4E-04 3.3E-04
CUI: C1266165
Disease: High grade surface osteosarcoma
High grade surface osteosarcoma 		0.700 0
dbSNP: rs386833845
rs386833845 		0.827 0.240 8 144514983 frameshift variant A/- del 2.4E-04 3.3E-04
CUI: C1849453
Disease: Rapadilino syndrome
Rapadilino syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs137853229
rs137853229 		0.851 0.240 8 144513412 stop gained G/A snv 1.2E-04 8.4E-05
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 1.000 7 1999 2016
dbSNP: rs137853229
rs137853229 		0.851 0.240 8 144513412 stop gained G/A snv 1.2E-04 8.4E-05
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities 0.700 1.000 5 2006 2015
dbSNP: rs137853229
rs137853229 		0.851 0.240 8 144513412 stop gained G/A snv 1.2E-04 8.4E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.700 1.000 5 2006 2015
dbSNP: rs137853229
rs137853229 		0.851 0.240 8 144513412 stop gained G/A snv 1.2E-04 8.4E-05
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs137853229
rs137853229 		0.851 0.240 8 144513412 stop gained G/A snv 1.2E-04 8.4E-05
CUI: C1849453
Disease: Rapadilino syndrome
Rapadilino syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs1085307090
rs1085307090 		0.882 0.240 8 144515325 splice donor variant C/A snv
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 2 2000 2003
dbSNP: rs1085307090
rs1085307090 		0.882 0.240 8 144515325 splice donor variant C/A snv
CUI: C1849453
Disease: Rapadilino syndrome
Rapadilino syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.700 1.000 2 2000 2003
dbSNP: rs1085307090
rs1085307090 		0.882 0.240 8 144515325 splice donor variant C/A snv
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 1.000 2 2000 2003
dbSNP: rs117642173
rs117642173 		0.925 0.160 8 144515243 splice acceptor variant C/T snv 3.6E-05 4.9E-05
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 1.000 4 2000 2017
dbSNP: rs386833844
rs386833844 		0.925 0.240 8 144515236 missense variant G/A snv 2.4E-05 1.4E-05
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 1.000 3 2008 2012
dbSNP: rs752729755
rs752729755 		0.925 0.160 8 144513109 frameshift variant AT/- del 2.8E-05
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 1.000 3 1999 2014
dbSNP: rs386833843
rs386833843 		0.925 0.240 8 144515324 splice donor variant A/- del 4.2E-04
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 1.000 2 2003 2003
dbSNP: rs386833851
rs386833851 		0.925 0.240 8 144513126 stop gained G/A snv 5.4E-05 4.3E-05
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 1.000 2 2003 2009
dbSNP: rs760363252
rs760363252 		0.925 0.160 8 144514441 splice donor variant C/T snv 4.1E-06
CUI: C0265308
Disease: Baller-Gerold syndrome
Baller-Gerold syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 1.000 2 2003 2003