Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 1
rs11652075
CARD14 ; SGSH
0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 1
rs963986
CAVIN1
1.000 0.040 17 42409561 intron variant G/C snv 0.15 1
rs130067
CCHCR1
0.851 0.200 6 31150734 missense variant T/G snv 0.23 0.21 2
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 1
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs10088247
CSMD1
1.000 0.040 8 3826677 intron variant C/T snv 0.76 1
rs7007032
CSMD1
1.000 0.040 8 3821924 intron variant C/T snv 0.75 1
rs11795343
DDX58
1.000 0.040 9 32523739 intron variant T/C snv 0.41 1
rs16841904
DENND1B
0.807 0.160 1 197732862 intron variant C/T snv 0.18 1
rs2700987
ELMO1
1.000 0.040 7 37346633 intron variant C/A snv 0.60 1
rs151823
ERAP1
1.000 0.040 5 96824289 intron variant A/C snv 0.90 1
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 1
rs27524
ERAP1 ; CAST
0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs3802826
ETS1
0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv 1
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 1