Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv 5
rs3130779 0.925 0.080 6 30904426 upstream gene variant A/C;G;T snv 5
rs3131034
DDR1
0.925 0.080 6 30886019 intron variant G/A snv 0.75 5
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 3
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 3
rs2856726 1.000 0.080 6 32698944 intergenic variant A/T snv 0.34 2
rs2858312 1.000 0.080 6 32699453 intergenic variant G/C snv 0.32 2
rs10214910
HLA-DPA1
1.000 0.080 6 33069898 intron variant C/A snv 0.23 0.32 1
rs10243492 1.000 0.080 7 32780825 intergenic variant A/G snv 0.48 1
rs1042169
HLA-DPA1 ; HLA-DPB1
1.000 0.080 6 33080909 missense variant G/A;T snv 0.31; 1.4E-02 1
rs1042190
HLA-DPA1
1.000 0.080 6 33069222 missense variant T/C snv 0.24 0.28 1
rs10484569 1.000 0.080 6 33091175 downstream gene variant G/A snv 5.9E-02 1
rs11089620
UBE2L3
1.000 0.080 22 21568167 non coding transcript exon variant C/G snv 0.18 1
rs1126542
HLA-DPA1
1.000 0.080 6 33069647 missense variant T/A;C;G snv 0.24 0.28 1
rs1126769
HLA-DPA1
1.000 0.080 6 33068658 missense variant T/G snv 0.24 0.29 1
rs11638027 1.000 0.080 15 90302268 intron variant G/T snv 9.9E-02 1
rs12484550
UBE2L3
1.000 0.080 22 21587626 intron variant C/T snv 0.18 1
rs12649554 1.000 0.080 4 100975519 regulatory region variant T/C snv 0.65 1
rs13213149
HLA-DPA1
1.000 0.080 6 33071909 intron variant T/C snv 0.28 1
rs1431399
HLA-DPA1
1.000 0.080 6 33073257 intron variant A/G;T snv 1
rs1431400
HLA-DPA1
1.000 0.080 6 33073399 intron variant C/T snv 0.29 1
rs1431401
HLA-DPA1
1.000 0.080 6 33073409 intron variant G/A snv 0.29 1
rs154977 1.000 0.080 6 32932241 downstream gene variant C/G;T snv 1
rs17056316 1.000 0.080 4 170892334 downstream gene variant A/G snv 2.6E-03 1