Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7916840 0.925 0.160 10 25424152 intron variant A/T snv 0.70 2
rs4097490 10 25497603 intron variant A/G snv 0.61 2
rs1754257 1.000 0.080 10 25385685 intron variant G/A snv 0.71 1
rs1360123 10 25484165 intron variant A/G snv 0.44 1
rs10508700 10 25532389 intron variant T/C snv 0.60 1
rs4749043 10 25533431 intron variant A/G snv 0.29 1
rs11014632 10 25588722 intron variant A/G snv 0.60 1
rs7077800 10 25530299 intron variant C/T snv 0.53 1
rs7086249 10 25522506 intron variant T/C snv 0.52 1