Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10051330
LINC02227
5 158392616 intron variant A/G;T snv 2
rs10066168
HAVCR1
5 157057207 intron variant C/G;T snv 2
rs10092965 8 8515975 intergenic variant A/G snv 0.43 2
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10176901
ABCB11
2 168974151 intron variant G/A snv 0.57 2
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10249276 7 118938630 intergenic variant A/G;T snv 1
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs10281955 7 118944637 intergenic variant G/A snv 0.86 1
rs10433415 3 133566686 intergenic variant G/T snv 0.57 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs1049296
TF
0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 4
rs10503387 8 9293015 intron variant C/T snv 0.33 2
rs10713774 4 26048829 intergenic variant C/- del 0.18 3
rs10734252 1.000 0.080 11 17383292 non coding transcript exon variant G/A snv 0.71 3
rs10741534 11 11233360 intergenic variant T/A;C snv 2
rs10744826
UBE3B
12 109527707 intron variant C/G snv 0.57 3
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs10761716 10 63122540 downstream gene variant C/G snv 0.40 3
rs10766309
SOX6
11 16235171 intron variant A/G;T snv 2
rs10769254
MYBPC3
11 47340914 intron variant G/C snv 0.27 4
rs10826334 10 59620724 intron variant C/A;G snv 3
rs10832961
SPTY2D1
11 18632410 intron variant C/G;T snv 2
rs10840138
MRPL23
11 1980665 intron variant T/C snv 8.3E-02 2
rs10841530
PDE3A
12 20446178 intron variant A/G snv 0.30 2