Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3738099 1.000 0.040 1 21568242 missense variant T/A;C snv 1
rs3767155 1.000 0.040 1 21558702 intron variant C/A;G;T snv 1
rs191940699 1.000 0.040 5 75620322 missense variant G/A;T snv 1
rs25957 1.000 0.040 5 14783123 intron variant C/G snv 0.77 1
rs27356 1.000 0.040 5 14722332 intron variant C/G;T snv 1
rs28006 1.000 0.040 5 14781635 intron variant T/C;G snv 1
rs26307 1.000 0.040 5 14705556 3 prime UTR variant T/C snv 0.72 1
rs4333130 1.000 0.040 4 80028675 intron variant C/G;T snv 1
rs4389526 1.000 0.040 4 80025321 intron variant T/A snv 0.59 1
rs4690127 1.000 0.040 4 79929167 intron variant T/C;G snv 1
rs6823031 1.000 0.040 4 79935302 intron variant C/T snv 1
rs6758317 1.000 0.040 2 233260305 intron variant C/T snv 0.24 1
rs17765610 1.000 0.040 6 89956054 intron variant A/G snv 9.0E-02 1
rs13209404 1.000 0.040 6 7909734 intron variant C/T snv 0.39 1
rs2150414 1.000 0.040 21 39243062 intron variant A/G snv 0.52 1
rs6517532 1.000 0.040 21 39270263 intron variant C/T snv 0.90 0.93 1
rs2171513 1.000 0.040 3 112466080 3 prime UTR variant A/G snv 0.86 0.76 1
rs1729674 1.000 0.040 2 61162602 missense variant T/G snv 0.41 0.44 1
rs7841425
CA1
1.000 0.040 8 85352584 intron variant C/A snv 1
rs10781500 1.000 0.040 9 136374886 upstream gene variant C/G;T snv 1
rs27037 1.000 0.040 5 96758990 intron variant T/G snv 0.72 1
rs13167972 1.000 0.040 5 96761124 3 prime UTR variant A/G snv 0.35 1
rs27582 1.000 0.040 5 96762510 3 prime UTR variant G/A snv 0.36 1
rs1055234 1.000 0.040 19 54154264 3 prime UTR variant G/A;C;T snv 1
rs11187265 1.000 0.040 10 93064409 missense variant G/A snv 0.10 8.8E-02 1