Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1388367359
rs1388367359
UBR1
1 1.000 0.360 15 43030063 missense variant G/A snv 7.0E-06 0.700 1.000 5 2005 2015
dbSNP: rs140972409
rs140972409
UBR1
1 1.000 0.360 15 42976795 missense variant A/G snv 1.2E-05 0.700 1.000 5 2005 2015
dbSNP: rs768686147
rs768686147
UBR1
1 1.000 0.360 15 43043376 missense variant G/T snv 8.0E-06 1.4E-05 0.700 1.000 5 2005 2015
dbSNP: rs1158249054
rs1158249054
UBR1
1 1.000 0.360 15 43056345 missense variant A/C snv 7.0E-06 0.700 0
dbSNP: rs119477054
rs119477054
UBR1
1 1.000 0.360 15 43082648 missense variant T/A;C snv 4.0E-06 0.700 0
dbSNP: rs119477055
rs119477055
UBR1
1 1.000 0.360 15 43048394 stop gained G/A snv 7.0E-06 0.700 0
dbSNP: rs1235541565
rs1235541565
UBR1
1 1.000 0.360 15 42998201 missense variant T/C snv 4.0E-06 2.1E-05 0.700 0
dbSNP: rs1480939799
rs1480939799
UBR1
1 1.000 0.360 15 42976806 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs797045112
rs797045112
UBR1
1 1.000 0.360 15 42983940 stop gained A/T snv 0.700 0