Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121965039
OAT
0.851 0.160 10 124408601 missense variant C/A;T snv 8.0E-06 6
rs121965059
OAT
0.925 0.080 10 124403892 missense variant G/A snv 1.6E-05 7.0E-06 4
rs121965047
OAT
0.925 0.080 10 124401746 missense variant C/T snv 4.0E-06 3
rs121965037
OAT
1.000 0.080 10 124412009 missense variant A/G snv 7.0E-06 2
rs121965038
OAT
1.000 0.080 10 124408887 missense variant C/A snv 2
rs121965040
OAT
1.000 0.080 10 124405545 missense variant C/G snv 7.2E-05 7.7E-05 2
rs121965041
OAT
1.000 0.080 10 124403019 missense variant C/G snv 2
rs121965042
OAT
1.000 0.080 10 124403015 missense variant C/T snv 2
rs121965043
OAT
1.000 0.080 10 124398057 missense variant A/C;G snv 4.0E-06; 2.7E-04 2
rs121965044
OAT
1.000 0.080 10 124398012 missense variant G/A snv 2.0E-05 4.9E-05 2
rs121965045
OAT
1.000 0.080 10 124400875 missense variant C/G snv 2
rs121965046
OAT
1.000 0.080 10 124403835 missense variant T/C snv 4.0E-06 1.4E-05 2
rs121965048
OAT
1.000 0.080 10 124412010 missense variant G/T snv 1.2E-05 1.4E-05 2
rs121965049
OAT
1.000 0.080 10 124401785 missense variant G/A snv 2
rs121965051
OAT
1.000 0.080 10 124403847 missense variant G/A;C snv 3.6E-05 2
rs121965052
OAT
1.000 0.080 10 124403820 missense variant C/G;T snv 4.8E-05 2
rs121965053
OAT
1.000 0.080 10 124400941 missense variant C/T snv 4.0E-05 7.0E-06 2
rs121965054
OAT
1.000 0.080 10 124398082 missense variant A/G snv 2
rs121965057
OAT
1.000 0.080 10 124402930 stop gained G/C snv 1.6E-05 2.8E-05 2
rs121965060
OAT
1.000 0.080 10 124408897 missense variant G/C snv 2
rs1800456
OAT
1.000 0.080 10 124397951 missense variant C/A;G;T snv 2.8E-04; 4.0E-06 2
rs267606925
OAT
1.000 0.080 10 124405488 missense variant G/T snv 8.0E-06 2.8E-05 2
rs386833597
OAT
1.000 0.080 10 124398081 missense variant C/T snv 2
rs386833598
OAT
1.000 0.080 10 124397955 missense variant A/T snv 1.2E-05 7.0E-06 2
rs386833599
OAT
1.000 0.080 10 124412013 frameshift variant G/- del 4.0E-06 2