Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9648724
PRKAG2 ; LOC644090
7 151805216 intron variant G/A snv 0.21 1
rs9341664 6 77375469 intergenic variant A/C snv 0.51 2
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs79666748 18 43280443 upstream gene variant A/C snv 7.0E-02 2
rs7935564
TRIM22 ; TRIM5
11 5697287 missense variant G/A snv 0.52 0.55 1
rs79056512
C5orf17
5 24063287 intron variant G/A snv 7.4E-02 2
rs7696218
PACRGL
4 20721189 intron variant G/A snv 0.11 2
rs765009973
CCR5AS ; CCR5
3 46373909 missense variant G/T snv 7.4E-05 2.1E-05 1
rs7640677 3 48340996 intergenic variant G/A snv 1.2E-02 1
rs7604115
UGT1A9 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A4
2 233749470 intron variant C/T snv 0.37 4
rs756207760
CXCR4
2 136115275 missense variant C/G;T snv 4.0E-06; 4.0E-06 2
rs75158213 3 48345739 intergenic variant T/C snv 1.2E-02 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs73670671
DLGAP2
8 1203645 intron variant T/C;G snv 2
rs731580
FGD5
3 14815331 intron variant G/A snv 0.31 2
rs73112098 5 67247451 regulatory region variant A/G snv 4.5E-02 1
rs73055087
C5orf17
5 24062454 intron variant C/A;T snv 2
rs73055009
C5orf17
5 24058406 intron variant A/G snv 7.5E-02 2
rs72749483 9 80670259 intergenic variant T/C snv 8.5E-02 2
rs72749479 9 80667356 intergenic variant T/C snv 8.5E-02 2
rs72609945 8 26048781 upstream gene variant C/A;T snv 0.13 2