Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001007
CCR5AS
0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs1002212321
RIMS2
1.000 0.040 8 103931366 missense variant T/C snv 1
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs1004234
LINC02863 ; IRF1-AS1
0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs10088247
CSMD1
1.000 0.040 8 3826677 intron variant C/T snv 0.76 1
rs1008953 1.000 0.040 20 45352086 upstream gene variant T/C snv 0.79 1
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 6
rs10180391
GNLY
1.000 0.040 2 85699222 downstream gene variant C/T snv 0.31 1
rs1020760
NFKB1
0.925 0.040 4 102593288 non coding transcript exon variant C/G snv 0.42 2
rs10405308 1.000 0.040 19 1312729 intergenic variant G/A snv 7.9E-02 1
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 11
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs10484879
IL17A
0.827 0.160 6 52187159 intron variant G/A;T snv 5
rs10489628
IL23R
1.000 0.040 1 67238424 intron variant G/A snv 0.43 1
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs10515778
LINC01932
1.000 0.040 5 159231004 intron variant A/G snv 0.13 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs1051738
PDE4A
1.000 0.040 19 10467167 missense variant C/A;T snv 0.17; 4.8E-05 1
rs1056198
RNF114
0.925 0.040 20 49939692 intron variant C/T snv 0.34 2
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1062470
PSORS1C1 ; CDSN
0.925 0.040 6 31116658 synonymous variant G/A snv 0.37 0.41 5
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5