Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 3
rs669408 1 232383404 regulatory region variant A/C snv 0.52 2
rs12730935
IL6R
1 154447416 intron variant G/A snv 0.27 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 4
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02 7
rs41272321
ACAD11 ; NPHP3-ACAD11
3 132619502 missense variant T/C;G snv 8.6E-06; 0.11 2
rs113341849 3 46342713 intergenic variant G/A snv 7.3E-02 1
rs115463265
RARB
3 24883579 intron variant C/T snv 2.4E-02 1
rs4303899
LINC02024
3 117682524 intron variant A/G snv 8.4E-02 1
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs16850073
CXCL6
4 73838282 3 prime UTR variant C/T snv 0.29 5
rs3733402
KLKB1
1.000 0.040 4 186236880 missense variant G/A;C snv 0.54 5
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43 3
rs9637599
PPM1K ; PPM1K-DT
4 88285078 intron variant A/C snv 0.56 3
rs1562064 4 145391948 intergenic variant G/A snv 0.74 2
rs184650103 4 73984932 upstream gene variant C/G;T snv 2
rs28645201
CCSER1
4 90607776 intron variant A/G snv 3.7E-02 2
rs34226052 4 88242371 intergenic variant A/G snv 0.22 2
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6
rs17159338
LINC01950
5 106942471 intron variant T/C snv 6.8E-02 2