Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2736172
PRRC2A ; SNORA38
0.882 0.160 6 31623121 non coding transcript exon variant C/T snv 0.41 0.29 6
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5