Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116965780 18 43300829 intergenic variant C/T snv 7.0E-02 2
rs11888459
UGT1A8 ; UGT1A5 ; UGT1A2P ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A9
2 233747994 non coding transcript exon variant T/C snv 0.37 4
rs11914494
IGSF11
3 119121264 intron variant G/A snv 1.8E-02 2
rs11926663
IGSF11
3 119125638 intron variant A/G snv 1.8E-02 2
rs12587266
RIN3
14 92580298 intron variant A/G snv 0.63 1
rs12662869
SLC17A1
0.925 0.120 6 25784253 intron variant C/A snv 0.34 4
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs139231591 3 48342403 regulatory region variant C/T snv 1.2E-02 1
rs1408270
SLC17A3
6 25872956 intron variant A/G snv 0.25 1
rs141827060
IGSF11
3 119132020 intron variant C/T snv 1.8E-02 2
rs1461494 11 123055777 downstream gene variant T/A;C snv 2
rs1552896
FREM1
9 14841389 intron variant C/A;G snv 1
rs16893073
C5orf17
5 24072508 intron variant C/G;T snv 2
rs17062789
DLGAP2
8 1203198 intron variant G/A;C snv 2
rs17062791
DLGAP2
8 1203431 intron variant C/T snv 0.14 2
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs17862875
UGT1A6 ; UGT1A10 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A9 ; UGT1A4 ; UGT1A7
2 233740656 intron variant G/A snv 0.30 4
rs17864701
UGT1A4 ; UGT1A3 ; UGT1A6 ; UGT1A8 ; UGT1A7 ; UGT1A5 ; DNAJB3 ; UGT1A9 ; UGT1A10
2 233744071 intron variant C/T snv 0.30 3
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1800450
MBL2
0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs1800452
CCR5AS ; CCR5
3 46373570 missense variant G/A snv 4.9E-03 1.9E-03 1
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46