Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73055009
C5orf17
5 24058406 intron variant A/G snv 7.5E-02 2
rs12587266
RIN3
14 92580298 intron variant A/G snv 0.63 1
rs1408270
SLC17A3
6 25872956 intron variant A/G snv 0.25 1
rs396716
FCGR3A
1 161544806 missense variant A/G snv 7.2E-05 6.3E-05 1
rs4349147
IL32
16 3074919 intron variant A/G snv 0.69 1
rs73112098 5 67247451 regulatory region variant A/G snv 4.5E-02 1
rs2586052
CUEDC1
17 57885718 5 prime UTR variant A/G;T snv 1
rs113051092
C5orf17
5 24060490 intron variant A/T snv 7.4E-02 2
rs638452 11 56495642 upstream gene variant A/T snv 0.58 2
rs67384697
HLA-C
1.000 0.040 6 31268906 3 prime UTR variant C/- delins 6.2E-04 2
rs11568350
SLC40A1
0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs12662869
SLC17A1
0.925 0.120 6 25784253 intron variant C/A snv 0.34 4
rs1552896
FREM1
9 14841389 intron variant C/A;G snv 1
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs2853699
CCR8
3 39332411 missense variant C/A;G;T snv 4.0E-06; 0.21; 2.8E-05 1
rs4435343 18 43322011 intergenic variant C/A;T snv 2
rs4936770
HSPA8 ; SNORD14E
11 123058167 intron variant C/A;T snv 2
rs72609945 8 26048781 upstream gene variant C/A;T snv 0.13 2
rs73055087
C5orf17
5 24062454 intron variant C/A;T snv 2
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs10929301
UGT1A6 ; UGT1A7 ; UGT1A5 ; UGT1A10 ; LOC100286922 ; UGT1A4 ; UGT1A9 ; UGT1A8 ; UGT1A3
2 233755003 splice region variant C/G;T snv 0.48 4
rs16893073
C5orf17
5 24072508 intron variant C/G;T snv 2
rs756207760
CXCR4
2 136115275 missense variant C/G;T snv 4.0E-06; 4.0E-06 2