Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 8
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs3766606
PARK7
0.827 0.120 1 7962137 intron variant G/T snv 0.22 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs2274907
ITLN1
0.851 0.200 1 160882036 missense variant A/G;T snv 0.66 5
rs11581607
IL23R
0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03 4
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 4
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 3
rs12103
INTS11 ; PUSL1 ; MIR6727
0.925 0.040 1 1312114 synonymous variant T/A;C;G snv 0.56 3
rs2488389
DENND1B
0.925 0.040 1 197662011 intron variant G/A snv 0.22 3
rs376377228
C1orf141 ; IL23R
0.925 0.040 1 67182950 missense variant A/G snv 1.6E-05 2.1E-05 3
rs41313262
IL23R
0.925 0.040 1 67240217 missense variant G/A;T snv 1.1E-02 1.0E-02 3
rs4656958
ITLN1
0.925 0.040 1 160887174 upstream gene variant A/G;T snv 3
rs6667605
LOC100996583
1.000 0.040 1 2571341 downstream gene variant C/T snv 0.53 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 3
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 3
rs758102857
C1orf141 ; IL23R
0.925 0.040 1 67206957 missense variant A/G snv 4.0E-06 3
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs10798069
PLA2G4A
1.000 0.040 1 186906327 intron variant G/T snv 0.37 2