Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10199914 2 238975165 regulatory region variant A/G snv 0.39 1
rs10438303 15 43724219 downstream gene variant T/C snv 0.16 1
rs10466588 11 116739533 regulatory region variant A/G snv 0.17 1
rs10474433 5 75321018 intron variant T/C snv 0.36 1
rs10475588 5 173227744 upstream gene variant T/C snv 2.1E-02 1
rs10495712 2 20973240 intergenic variant A/G snv 0.77 1
rs10853981 19 4965053 upstream gene variant G/A;C snv 1
rs11066600 12 113552405 intergenic variant A/G snv 0.46 1
rs11230873 11 62024805 intergenic variant A/G snv 7.0E-02 1
rs11654954 17 39589726 intergenic variant A/G;T snv 1
rs11745702 5 133108609 downstream gene variant T/C snv 0.23 1
rs11780610 8 18402366 downstream gene variant C/T snv 0.70 1
rs12206516 6 20506584 intergenic variant A/G snv 0.15 1
rs12307997 12 7702675 intergenic variant G/A snv 0.85 1
rs12326039 17 73155324 intergenic variant G/T snv 1.9E-02 1
rs12448528 16 56951643 TF binding site variant A/G snv 0.82 1
rs12678799 8 125458589 intergenic variant C/T snv 0.20 1
rs12679189 8 125461323 intergenic variant T/C snv 0.21 1
rs12771265 10 69651450 regulatory region variant G/A snv 0.44 1
rs12992267 2 20992773 regulatory region variant C/T snv 0.26 1
rs13198641 6 126863842 intron variant A/T snv 0.36 1
rs138754224 18 71161939 intron variant T/C snv 1.3E-02 1
rs139441335 7 73748480 intergenic variant A/G snv 1.7E-02 1
rs1429974 2 21077898 intergenic variant C/A;T snv 1
rs149217485 2 27423411 upstream gene variant T/C snv 1.6E-03 1