Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9260620 6 29955314 upstream gene variant T/G snv 0.24 7
rs7758512 1.000 6 30002812 intron variant T/G snv 0.17 4
rs3893464 1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46 3
rs115625073 1.000 0.040 6 29924456 upstream gene variant T/C snv 2
rs2524005 0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 2
rs114204022 1.000 0.040 6 29972902 upstream gene variant G/A snv 2
rs113205291 1.000 0.040 6 29894844 upstream gene variant A/G;T snv 2
rs115960997 1.000 0.040 6 29934332 downstream gene variant G/A;T snv 2
rs111312615 1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs144304366 1.000 0.040 6 29936216 downstream gene variant T/C snv 2
rs114950038 1.000 0.040 6 29983056 downstream gene variant G/A;C snv 2
rs9260151 1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14 2
rs9260313 6 29949108 downstream gene variant T/C snv 0.42 2
rs9260489 1.000 0.080 6 29952555 upstream gene variant T/A;G snv 2
rs7749944 0.925 6 29992223 upstream gene variant A/C snv 1.3E-02 2
rs192543598 6 29963568 downstream gene variant A/G snv 1.6E-02 2
rs2523961 0.925 0.120 6 29971803 non coding transcript exon variant G/A snv 0.16 2
rs4313034 0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78 2
rs115559990 6 29926633 non coding transcript exon variant C/G;T snv 1
rs2523946 0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv 1
rs3823355 1.000 0.040 6 29974306 upstream gene variant C/A;T snv 1
rs6914699 6 29966245 downstream gene variant T/C snv 0.41 1
rs2523933 6 29964515 intergenic variant G/C;T snv 1
rs2571400 6 29959945 downstream gene variant C/G snv 0.51 1
rs3893463 6 29967628 downstream gene variant C/T snv 0.41 1