Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9368726 6 32470765 intron variant T/C snv 0.29 1
rs9405108 6 32470871 intron variant C/T snv 0.29 1
rs10947262 0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 3
rs12759054 1.000 0.040 1 233984064 intron variant T/A;C snv 3
rs2294881 1.000 0.040 6 32399827 intron variant T/C snv 0.19 3
rs2213585 1.000 0.040 6 32445373 downstream gene variant G/A snv 0.61 2
rs2213586 1.000 0.040 6 32445317 downstream gene variant A/G snv 0.61 2
rs28362683 1.000 0.040 6 32405186 synonymous variant G/A snv 0.12 0.10 2
rs4248166 1.000 0.040 6 32398644 intron variant T/C snv 0.18 2
rs7195 1.000 0.040 6 32444762 3 prime UTR variant A/G snv 0.61 2
rs7754768 1.000 0.040 6 32452402 regulatory region variant C/T snv 0.56 2
rs9268658 1.000 0.040 6 32442939 intron variant G/A;C snv 2
rs4935356 1.000 0.080 6 32444611 intron variant T/A;G snv 2
rs204994 0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 4
rs2854275 0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02 4
rs28366298 0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs3130048 1.000 0.120 6 31645962 intron variant T/C snv 0.23 3
rs204995 1.000 0.120 6 32186508 non coding transcript exon variant A/G snv 0.21 0.27 2
rs2736157 1.000 0.120 6 31633043 intron variant A/G;T snv 0.15 0.17 2
rs3130626 1.000 0.120 6 31630712 synonymous variant A/G snv 0.15 0.17 2
rs3130628 1.000 0.120 6 31641495 non coding transcript exon variant T/C snv 0.15 0.18 2
rs6901541 1.000 0.120 6 32474484 upstream gene variant T/C;G snv 2
rs8084 1.000 0.120 6 32443258 splice acceptor variant A/C;T snv 0.61; 8.1E-06 2
rs9267532 1.000 0.120 6 31672202 missense variant C/T snv 7.4E-02 7.9E-02 2
rs1048369 0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 4