Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs372292910
PCDHB4
1.000 0.040 5 141122905 frameshift variant A/-;AA delins 1.7E-04 3
rs6755571
UGT1A8 ; UGT1A6 ; UGT1A10 ; UGT1A7 ; UGT1A9 ; UGT1A5 ; UGT1A4
1.000 0.040 2 233718890 missense variant C/A;T snv 3.6E-02; 4.0E-06 3
rs74315322
HAX1
1.000 0.040 1 154275165 stop gained C/T snv 3.6E-05 3
rs10157763
AKT3
1.000 0.040 1 243831739 intron variant T/A;C snv 2
rs11663316 1.000 0.040 18 9027916 intergenic variant T/A snv 0.34 2
rs1178326
HDAC9
1.000 0.040 7 18195234 intron variant T/C snv 3.9E-02 2
rs118166657 1.000 0.040 14 63580544 intergenic variant C/G snv 1.3E-02 2
rs12668095
LOC105375268
1.000 0.040 7 47036178 intron variant G/A;C snv 2
rs13287547
C9orf92
1.000 0.040 9 16286892 intron variant A/G snv 0.32 2
rs139427007
LOC105369927 ; LOC105369928
1.000 0.040 12 97202325 intergenic variant A/T snv 6.3E-05 2
rs141860749
SYT2
1.000 0.040 1 202668176 intron variant C/A snv 2.7E-04 2
rs1429264
COTL1
1.000 0.040 16 84589878 intron variant T/C snv 0.28 2
rs143543475 1.000 0.040 10 27419100 upstream gene variant G/C snv 8.0E-02 2
rs146173241 1.000 0.040 10 116285226 downstream gene variant C/T snv 7.1E-03 2
rs148173957
LOC105378976
1.000 0.040 5 56078195 intron variant TT/- del 8.2E-02 2
rs150435906
LOC107986950
1.000 0.040 8 65952103 intergenic variant G/T snv 2.7E-04 2
rs17084405 1.000 0.040 18 71429162 intergenic variant G/A snv 0.13 2
rs199542988
FOXRED1
1.000 0.040 11 126277489 missense variant G/A;T snv 1.2E-05; 4.0E-06 2
rs2279020
GABRA1
1.000 0.040 5 161895883 non coding transcript exon variant G/A snv 0.62 0.63 2
rs28898617
UGT1A8 ; UGT1A10 ; UGT1A3 ; UGT1A7 ; UGT1A4 ; UGT1A9 ; UGT1A5 ; UGT1A6
1.000 0.040 2 233729143 missense variant A/G snv 3.5E-03 1.1E-03 2
rs2930491 1.000 0.040 8 106830066 intergenic variant C/G;T snv 0.20 2
rs55949311
LOC105370210
1.000 0.040 13 53557781 intron variant G/A;T snv 2
rs62270313
EPHB1
1.000 0.040 3 134930924 intron variant T/C snv 0.16 2
rs631844
LINC02109 ; LOC107986410
1.000 0.040 5 29054513 intron variant C/T snv 0.48 2
rs71568191 1.000 0.040 6 104230957 intergenic variant G/A snv 8.1E-02 2