Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50 3
rs532098
HLA-DRB1
0.882 0.120 6 32610275 intergenic variant G/A snv 0.43 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs3134945
RNF5 ; MIR6833 ; AGPAT1
0.827 0.240 6 32178715 intron variant C/A snv 0.18 3
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs3094061 0.925 0.160 6 30353412 downstream gene variant A/C;T snv 2
rs3130284
AGPAT1
0.925 0.120 6 32172710 intron variant T/C snv 0.18 2
rs3134947
AGPAT1 ; RNF5
0.925 0.120 6 32177428 intron variant C/T snv 0.18 2
rs3757247
BACH2
0.827 0.320 6 90247744 intron variant C/T snv 0.38 2
rs28362683
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32405186 synonymous variant G/A snv 0.12 0.10 2
rs229527
C1QTNF6
0.925 0.160 22 37185445 missense variant C/A;G snv 0.43 2
rs130065
CCHCR1
0.925 0.120 6 31154723 missense variant G/A snv 0.15 0.16 2
rs1635168
HERC2
1.000 0.040 15 28290120 intron variant A/C snv 0.77 2
rs6904029
HLA-A ; HCG9
0.851 0.200 6 29975290 non coding transcript exon variant G/A snv 0.29 0.26 2
rs2858870
HLA-DRB1
0.851 0.280 6 32604474 intergenic variant T/A;C snv 2
rs1264350
LINC00243
0.925 0.160 6 30828768 intron variant T/C snv 9.4E-02 2
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs1847134
LOC107984363 ; TYR
0.925 0.080 11 89272085 intron variant A/C snv 0.26 2
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44 2
rs13091753
LPP
1.000 0.040 3 188396801 intron variant G/C;T snv 2
rs1559810
LPP
1.000 0.040 3 188406566 intron variant C/A snv 0.36 2
rs9851967
LPP
1.000 0.040 3 188369840 intron variant C/T snv 0.35 2
rs1265159
POU5F1
0.882 0.240 6 31172270 intron variant G/A snv 0.21 2
rs3096697
PPT2-EGFL8 ; PPT2 ; EGFL8
0.882 0.200 6 32166733 missense variant G/A snv 0.16 0.18 2
rs1079541 1.000 0.040 6 30438979 intergenic variant C/A snv 0.17 1