Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2431820 1.000 0.080 19 10024608 downstream gene variant T/C snv 8.0E-02 1
rs879254375 0.925 0.080 19 11089414 upstream gene variant C/A;G snv 7.0E-06 4
rs1555800611 1.000 0.080 19 11089319 upstream gene variant GGGTTAAAAAGCCGATGTCACATCGGCCGTTCGAAACTCCTCCTCTTGCAGTGAGGTGAAGACATTTGAAAATCACCCCACTGCAAACTCCTCCCCCTGCTAGAAACCTCACATTGAAATGCTGTAAATGACGTGGGCCC/- delins 3
rs875989887 0.925 0.080 19 11089409 upstream gene variant C/A;G;T snv 3
rs878854023 1.000 0.080 19 11089361 upstream gene variant C/T snv 3
rs879254370 1.000 0.080 19 11089407 upstream gene variant C/G;T snv 3
rs944580031 1.000 0.080 19 11089452 upstream gene variant G/A;C snv 3
rs989307060 1.000 0.080 19 11089263 upstream gene variant C/G snv 2.8E-05 3
rs387906307 0.925 0.080 19 11089411 upstream gene variant T/- del 2
rs1555800620 1.000 0.080 19 11089356 upstream gene variant CTCCTCC/TG delins 1
rs1555800629 1.000 0.080 19 11089377 upstream gene variant G/A snv 1
rs1555800631 1.000 0.080 19 11089398 upstream gene variant C/G snv 1
rs1555800632 1.000 0.080 19 11089399 upstream gene variant A/G snv 1
rs1555800648 1.000 0.080 19 11089451 upstream gene variant C/T snv 1
rs7259203 1.000 0.080 19 8701483 upstream gene variant T/C;G snv 1
rs747068848 1.000 0.080 19 11089448 upstream gene variant T/C snv 1
rs777716188 1.000 0.080 19 11089428 upstream gene variant T/C snv 2.8E-05 1
rs875989886 1.000 0.080 19 11089429 upstream gene variant C/T snv 7.0E-06 1
rs879254363 1.000 0.080 19 11089363 upstream gene variant CTT/- delins 1
rs879254364 1.000 0.080 19 11089393 upstream gene variant C/T snv 1
rs879254365 1.000 0.080 19 11089394 upstream gene variant AC/TTCTGCAAACTCCT delins 1
rs879254367 1.000 0.080 19 11089397 upstream gene variant C/T snv 1
rs879254371 1.000 0.080 19 11089410 upstream gene variant C/A;G snv 1
rs879254372 1.000 0.080 19 11089411 upstream gene variant T/C snv 1
rs879254374 1.000 0.080 19 11089413 upstream gene variant C/G;T snv 1