Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 9
rs63751163 0.807 0.120 14 73192844 missense variant T/C snv 7