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: rs747240928
rs747240928
1.000 0.120 8 43196999 stop gained C/T snv 1.2E-05 7.0E-06
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 3 2006 2015
dbSNP: rs775078211
rs775078211
0.882 0.120 8 43191495 stop gained C/G;T snv 4.0E-06; 1.6E-05
CUI: C0026706
Disease: Mucopolysaccharidosis III
Mucopolysaccharidosis III
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 3 2006 2008
dbSNP: rs1554537841
rs1554537841
1.000 0.120 8 43197900 stop gained C/G snv
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 2 2009 2015
dbSNP: rs1563366896
rs1563366896
0.882 0.120 8 43169216 stop gained C/T snv
CUI: C0026706
Disease: Mucopolysaccharidosis III
Mucopolysaccharidosis III
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 2 2008 2015
dbSNP: rs775078211
rs775078211
0.882 0.120 8 43191495 stop gained C/G;T snv 4.0E-06; 1.6E-05
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 2 2006 2013
dbSNP: rs775078211
rs775078211
0.882 0.120 8 43191495 stop gained C/G;T snv 4.0E-06; 1.6E-05
CUI: C4225287
Disease: RETINITIS PIGMENTOSA 73
RETINITIS PIGMENTOSA 73
0.700 1.000 2 2006 2013
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs1554533211
rs1554533211
1.000 0.120 8 43178169 stop gained G/A snv
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 1 2006 2006
dbSNP: rs1563366896
rs1563366896
0.882 0.120 8 43169216 stop gained C/T snv
CUI: C4225287
Disease: RETINITIS PIGMENTOSA 73
RETINITIS PIGMENTOSA 73
0.700 1.000 1 2008 2008
dbSNP: rs1563366896
rs1563366896
0.882 0.120 8 43169216 stop gained C/T snv
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 1 2008 2008
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.700 0
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C0086795
Disease: Pfaundler-Hurler Syndrome
Pfaundler-Hurler Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C1832451
Disease: Cranial hyperostosis
Cranial hyperostosis
Musculoskeletal Diseases 0.700 0
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C2243051
Disease: Large head (disorder)
Large head (disorder)
0.700 0
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C1850041
Disease: Facial hirsutism
Facial hirsutism
0.700 0
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C0013528
Disease: Echolalia
Echolalia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.700 0
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
Delayed speech and language development
Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1057518644
rs1057518644
0.925 0.120 8 43192413 stop gained C/T snv
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
Pathological Conditions, Signs and Symptoms 0.700 0
dbSNP: rs121908283
rs121908283
1.000 0.120 8 43178184 stop gained T/G snv
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs372933126
rs372933126
0.925 0.120 8 43178109 stop gained C/A;T snv 1.3E-04 2.1E-05
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs372933126
rs372933126
0.925 0.120 8 43178109 stop gained C/A;T snv 1.3E-04 2.1E-05
CUI: C4225287
Disease: RETINITIS PIGMENTOSA 73
RETINITIS PIGMENTOSA 73
0.700 0
dbSNP: rs121908285
rs121908285
0.925 0.120 8 43182162 missense variant C/T snv 1.2E-05 7.0E-06
CUI: C4225287
Disease: RETINITIS PIGMENTOSA 73
RETINITIS PIGMENTOSA 73
0.700 1.000 5 2006 2011
dbSNP: rs121908285
rs121908285
0.925 0.120 8 43182162 missense variant C/T snv 1.2E-05 7.0E-06
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 5 2006 2011
dbSNP: rs753355844
rs753355844
0.882 0.120 8 43193790 missense variant G/A snv 1.6E-05
CUI: C0086649
Disease: MPS III C
MPS III C
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 5 2006 2010