Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9461219 0.882 0.160 6 25836699 intron variant C/G;T snv 3
rs9556958 1.000 0.040 13 98447792 3 prime UTR variant C/G;T snv 3
rs9636107 1.000 0.040 18 55532886 intron variant A/G;T snv 3
rs9841504 0.827 0.120 3 114643917 intron variant C/G;T snv 3
rs10061788 1.000 0.040 5 88638889 intron variant G/A;T snv 2
rs1024582 1.000 0.040 12 2293080 intron variant A/G;T snv 2
rs10520163 1.000 0.040 4 169705401 intron variant T/A;C snv 2
rs10757417 1.000 0.040 9 23347855 intron variant G/A;T snv 2
rs1076884 1.000 0.040 16 13653946 intergenic variant C/G;T snv 2
rs10961430 1.000 0.040 9 14224064 intron variant G/C;T snv 2
rs11130 1.000 0.040 16 15724453 3 prime UTR variant G/A;C snv 0.56; 4.0E-06 2
rs111312615 1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs11166628 1.000 0.040 8 136066082 intron variant G/A;C snv 2
rs111977918 1.000 0.040 6 31268274 downstream gene variant G/A;C snv 2
rs112209031 1.000 0.040 6 32524630 intron variant T/C;G snv 2
rs1131275 1.000 0.040 6 31356183 missense variant G/A;C snv 0.68 2
rs113205291 1.000 0.040 6 29894844 upstream gene variant A/G;T snv 2
rs113397282 1.000 0.040 6 32520273 intron variant T/C;G snv 2
rs114041423 1.000 0.040 6 29639270 upstream gene variant G/A snv 2
rs114086406 1.000 0.040 6 32374760 intron variant G/A snv 2
rs114115252 1.000 0.040 6 30931418 3 prime UTR variant G/A;C;T snv 2
rs114142645 1.000 0.040 6 31245806 regulatory region variant T/C snv 2
rs114204022 1.000 0.040 6 29972902 upstream gene variant G/A snv 2
rs114274203 1.000 0.040 6 31300843 intron variant C/T snv 2
rs114276265 1.000 0.040 6 31219298 upstream gene variant C/T snv 2