Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 13 2011 2017
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5
0.700 1.000 13 2010 2017
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
Mitochondrial Complex II Deficiency
0.700 1.000 9 2011 2016
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.700 1.000 4 2010 2017
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C1849265
Disease: Overgrowth
Overgrowth
0.700 1.000 4 2010 2017
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.700 1.000 4 2010 2017
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
Attention deficit hyperactivity disorder
0.700 1.000 4 2010 2017
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma
0.010 1.000 1 2015 2015
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C0030421
Disease: Paraganglioma
Paraganglioma
0.010 1.000 1 2015 2015
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma
0.010 1.000 1 2015 2015
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C0334583
Disease: Pilocytic Astrocytoma
Pilocytic Astrocytoma
0.700 0
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C3203483
Disease: Pulmonary chondroma
Pulmonary chondroma
0.700 0
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C3150898
Disease: CARDIOMYOPATHY, DILATED, 1GG
CARDIOMYOPATHY, DILATED, 1GG
0.700 0
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C1858592
Disease: Carney Triad
Carney Triad
0.700 0
dbSNP: rs142441643
rs142441643
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
0.700 0
dbSNP: rs750380279
rs750380279
0.851 0.200 5 218357 start lost T/A;C;G snv 8.7E-06; 8.7E-06
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5
0.700 1.000 4 2000 2016
dbSNP: rs750380279
rs750380279
0.851 0.200 5 218357 start lost T/A;C;G snv 8.7E-06; 8.7E-06
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
Mitochondrial Complex II Deficiency
0.700 1.000 4 2000 2016
dbSNP: rs750380279
rs750380279
0.851 0.200 5 218357 start lost T/A;C;G snv 8.7E-06; 8.7E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2015 2015
dbSNP: rs750380279
rs750380279
0.851 0.200 5 218357 start lost T/A;C;G snv 8.7E-06; 8.7E-06
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs750380279
rs750380279
0.851 0.200 5 218357 start lost T/A;C;G snv 8.7E-06; 8.7E-06
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors
0.010 1.000 1 2019 2019
dbSNP: rs750380279
rs750380279
0.851 0.200 5 218357 start lost T/A;C;G snv 8.7E-06; 8.7E-06
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs9809219
rs9809219
0.925 0.120 5 251100 missense variant C/T snv 4.0E-05 1.4E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 10 1995 2017
dbSNP: rs387906780
rs387906780
0.882 0.120 5 251439 missense variant C/T snv 1.2E-05 2.1E-05
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5
0.800 1.000 8 2010 2017
dbSNP: rs387906780
rs387906780
0.882 0.120 5 251439 missense variant C/T snv 1.2E-05 2.1E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 7 2009 2014
dbSNP: rs387906780
rs387906780
0.882 0.120 5 251439 missense variant C/T snv 1.2E-05 2.1E-05
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
Mitochondrial Complex II Deficiency
0.700 1.000 7 2010 2017