Source: CLINVAR

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: rs387906662
rs387906662
1.000 0.040 5 150056071 missense variant C/A snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.800 1.000 0 2011 2014
dbSNP: rs281860281
rs281860281
1.000 0.040 5 150056316 missense variant C/A;T snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.730 1.000 0 2013 2015
dbSNP: rs587777247
rs587777247
1.000 0.040 5 150056319 missense variant G/A;T snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.710 1.000 4 2013 2016
dbSNP: rs397515556
rs397515556
1.000 0.040 5 150056332 missense variant G/A snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.710 1.000 1 2012 2013
dbSNP: rs281860270
rs281860270
1.000 0.040 5 150057309 missense variant A/G snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.710 1.000 0 2013 2013
dbSNP: rs281860274
rs281860274
1.000 0.040 5 150056280 missense variant A/G snv 4.0E-06
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.710 1.000 0 2012 2012
dbSNP: rs281860279
rs281860279
1.000 0.040 5 150055267 missense variant A/G snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.710 1.000 0 2013 2013
dbSNP: rs917027829
rs917027829
1.000 5 150069942 stop gained G/A;T snv 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 13 1984 2014
dbSNP: rs917027829
rs917027829
1.000 5 150069942 stop gained G/A;T snv 4.0E-06
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 13 1984 2014
dbSNP: rs917027829
rs917027829
1.000 5 150069942 stop gained G/A;T snv 4.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 13 1984 2014
dbSNP: rs690016548
rs690016548
0.925 0.080 5 150056331 missense variant C/T snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.700 1.000 2 2013 2013
dbSNP: rs1057519802
rs1057519802
5 150061765 missense variant A/C snv
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519802
rs1057519802
5 150061765 missense variant A/C snv
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease
0.700 1.000 1 2009 2009
dbSNP: rs1057520014
rs1057520014
5 150073480 missense variant C/A snv
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.700 1.000 1 1990 1990
dbSNP: rs121913390
rs121913390
5 150073481 stop gained A/G;T snv
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.700 1.000 1 1990 1990
dbSNP: rs121913390
rs121913390
5 150073481 stop gained A/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913392
rs121913392
5 150054081 stop gained A/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913393
rs121913393
5 150054083 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913393
rs121913393
5 150054083 missense variant A/G snv
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.700 1.000 1 1990 1990
dbSNP: rs1801271
rs1801271
5 150054082 missense variant T/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1801271
rs1801271
5 150054082 missense variant T/A;C snv
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.700 1.000 1 1990 1990
dbSNP: rs587777245
rs587777245
1.000 0.040 5 150059771 frameshift variant -/A delins
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.700 1.000 1 2014 2014
dbSNP: rs587777246
rs587777246
1.000 0.040 5 150056218 splice donor variant C/A snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.700 1.000 1 2014 2014
dbSNP: rs690016546
rs690016546
1.000 0.040 5 150061777 frameshift variant T/- del
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.700 1.000 1 2013 2013
dbSNP: rs690016547
rs690016547
1.000 0.040 5 150060942 missense variant A/C snv
Hereditary Diffuse Leukoencephalopathy with Spheroids
0.700 1.000 1 2013 2013