Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35808169 0.776 0.080 12 4259441 intron variant T/C snv 0.17 10
rs10774214 0.790 0.080 12 4259186 intron variant T/C snv 0.54 9
rs4572213 0.790 0.080 12 4256383 intron variant A/T snv 0.10 9
rs12818766 0.790 0.080 12 4266925 intron variant G/A snv 0.17 9
rs76895963 1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs71061176 12 4269579 intron variant -/T ins 0.18 1
rs11063069 0.925 0.080 12 4265207 intron variant A/G snv 0.20 1