Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4946935
FOXO3
1.000 0.040 6 108679539 intron variant A/G snv 0.54 2
rs6610650 1.000 0.040 X 37777261 intron variant G/A snv 0.27 2
rs73226617
LINC02618
0.925 0.040 3 141681811 intron variant G/A snv 4.4E-02 2
rs755850200
VDR
1.000 0.040 12 47846347 missense variant T/C snv 2.1E-05 7.0E-06 2
rs772717932
IL1B
1.000 0.040 2 112830530 missense variant C/A;T snv 4.0E-06; 1.6E-05 2
rs80292941
CYTOR ; LOC101928152
1.000 0.040 2 87480257 non coding transcript exon variant A/T snv 0.16 2
rs8073782 0.925 0.040 17 27807685 intron variant C/T snv 0.27 2
rs9373523
STXBP5
1.000 0.040 6 147379997 intron variant T/G snv 0.62 2
rs10051924
IRGM
1.000 0.040 5 150847077 5 prime UTR variant T/C snv 0.21 1
rs1017281
ASAP1
1.000 0.040 8 130234967 intron variant G/A snv 0.37 1
rs1045481
GEMIN4
1.000 0.040 17 744917 missense variant G/A;C snv 0.20 1
rs10507172
HSP90B1 ; C12orf73
1.000 0.040 12 103949490 intron variant G/A snv 7.2E-02 1
rs10507173
HSP90B1 ; C12orf73
1.000 0.040 12 103950058 intron variant A/G snv 6.3E-02 1
rs1052677
POLD1 ; NR1H2
1.000 0.040 19 50382924 3 prime UTR variant C/G;T snv 0.45 1
rs1059225
SFTPA1
1.000 0.040 10 79615230 3 prime UTR variant T/C snv 0.47 1
rs1075309 1.000 0.040 2 5113465 intergenic variant C/T snv 0.20 1
rs10911362
NCF2 ; SMG7
1.000 0.040 1 183579857 intron variant A/G snv 0.12 1
rs10956514
ASAP1
1.000 0.040 8 130240512 intron variant A/G snv 0.37 1
rs1101998
IFI16
1.000 0.040 1 159029494 intron variant C/T snv 0.65 1
rs11031728 1.000 0.040 11 32342070 intron variant C/G snv 0.18 1
rs11040
TENT5A
1.000 0.040 6 81752132 missense variant C/A;G;T snv 1
rs11117415
MIR6774 ; IRF8
1.000 0.040 16 85917080 intron variant A/G snv 0.12 1
rs11246213
IRF7
1.000 0.040 11 612967 intron variant A/G snv 0.25 0.33 1
rs11556887
SP110 ; SP140
1.000 0.040 2 230212961 missense variant G/A snv 0.10 7.4E-02 1
rs11567764
IL7R
1.000 0.040 5 35873503 missense variant G/A;T snv 9.5E-03; 4.0E-06 1