Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs963986
CAVIN1
1.000 0.040 17 42409561 intron variant G/C snv 0.15 1
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 3
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 2
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 2
rs1250544
ZMIZ1
0.882 0.080 10 79273128 intron variant G/A snv 0.32 1
rs181359
UBE2L3
0.882 0.080 22 21574352 intron variant G/A snv 0.21 1
rs2066807
STAT2
0.925 0.080 12 56346898 missense variant C/G snv 4.9E-02 4.6E-02 1
rs3213094
IL12B ; LOC107986469
0.925 0.080 5 159323761 intron variant C/G;T snv 0.26 1
rs458017
MFSD4B ; REV3L
0.925 0.080 6 111374888 missense variant T/C snv 5.9E-02 5.6E-02 1
rs8016947 0.925 0.080 14 35363460 intron variant T/G snv 0.60 1
rs999556 0.925 0.080 5 151094113 upstream gene variant A/G snv 0.38 1
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 5
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs702873
LINC01185
0.882 0.120 2 60854407 intron variant C/T snv 0.35 3
rs10852936
ZPBP2
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 2
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 2
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 2
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 2
rs2082412 0.925 0.120 5 159290781 downstream gene variant G/A snv 0.27 2
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv 2
rs492602
LOC105447645 ; FUT2
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 2
rs495337
SPATA2
0.925 0.120 20 49905793 synonymous variant G/A snv 0.44 0.35 2
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 2
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 2
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 1