Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10994856
A1CF
0.925 0.120 10 50885488 intron variant G/A snv 0.19 5
rs10994860
A1CF
0.925 0.120 10 50885664 5 prime UTR variant C/T snv 0.19 5
rs10821905
A1CF
0.925 0.120 10 50886333 upstream gene variant G/A;T snv 4
rs41274050
ASAH2B ; A1CF
10 50814012 missense variant C/A;T snv 4.0E-06; 5.3E-03 4
rs10821871
A1CF
0.882 0.160 10 50824350 intron variant T/C snv 0.22 3
rs10994720
A1CF
0.882 0.160 10 50852341 intron variant G/A snv 0.21 3
rs11815391
A1CF
0.882 0.160 10 50818978 intron variant A/G snv 0.26 3
rs10821877
A1CF
0.925 0.120 10 50843899 intron variant C/T snv 0.20 2
rs10994731
A1CF
0.925 0.120 10 50854429 intron variant A/G snv 8.4E-02 2
rs12768968
A1CF
0.925 0.120 10 50861992 intron variant G/C snv 0.20 2
rs17592117
A1CF
0.925 0.120 10 50883278 intron variant T/C;G snv 2
rs3808919
A1CF
0.925 0.120 10 50886584 upstream gene variant A/G snv 0.46 2
rs4567398
A1CF
0.925 0.120 10 50857162 intron variant C/T snv 8.5E-02 2
rs10821876
A1CF
1.000 0.040 10 50843482 intron variant T/A;C snv 1
rs12243360
A1CF
1.000 0.040 10 50848012 intron variant C/T snv 5.2E-02 1
rs12266425
A1CF
1.000 0.040 10 50866013 intron variant A/G snv 9.9E-03 1
rs12769066
A1CF
1.000 0.040 10 50852902 intron variant C/T snv 0.22 1
rs17500631
A1CF
1.000 0.040 10 50867812 intron variant G/T snv 0.12 1
rs4488147
A1CF
1.000 0.040 10 50837871 intron variant C/T snv 2.2E-02 1
rs750443908
A1CF
1.000 0.080 10 50859904 missense variant C/A;T snv 6.0E-05; 8.0E-06 1
rs4256922
ASAH2B ; A1CF
10 50808856 intron variant T/C;G snv 1