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: rs149079426
rs149079426
TRIP11
2 1.000 0.120 14 92021558 stop gained G/A;C snv 4.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs1566843321
rs1566843321
TRIP11
2 1.000 0.120 14 91975213 missense variant T/C snv 0.700 1.000 1 2019 2019
dbSNP: rs1566863801
rs1566863801
TRIP11
2 1.000 0.120 14 92011072 missense variant C/A snv 0.700 1.000 1 2019 2019
dbSNP: rs267607138
rs267607138
TRIP11
2 0.925 0.120 14 92015729 stop gained G/A;T snv 2.0E-05 0.700 1.000 1 2019 2019
dbSNP: rs780625551
rs780625551
TRIP11
2 1.000 0.120 14 92003442 stop gained G/A;C snv 4.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs1400419650
rs1400419650
TRIP11
38 0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs1555386022
rs1555386022
TRIP11
38 0.708 0.320 14 92003418 splice donor variant C/A snv 0.700 0