Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10043077 5 56397112 intergenic variant T/C snv 0.29 1
rs1012089 16 74138074 intron variant C/G;T snv 0.40 1
rs10158347 1 232393998 downstream gene variant A/G snv 0.31 1
rs10160382 11 76416170 downstream gene variant T/C snv 0.39 1
rs10182056 2 55463087 intergenic variant A/G snv 0.30 1
rs10203824 2 190731124 intergenic variant A/C snv 0.22 1
rs1020661 5 57883677 intergenic variant T/C snv 0.63 1
rs10233127 7 30893838 intron variant T/A snv 0.23 1
rs10460108 18 75322196 intergenic variant A/G snv 0.51 1
rs10521146 17 6570339 regulatory region variant C/T snv 0.45 1
rs10712836 8 125498975 intron variant A/- delins 0.48 1
rs10736586 11 130598201 intergenic variant C/G;T snv 1
rs10787517 10 114055047 intergenic variant T/A;C snv 1
rs10818962 9 124420014 upstream gene variant C/G snv 0.36 1
rs10832013 11 13273806 upstream gene variant G/T snv 0.55 1
rs10841376 12 19826947 intron variant C/G snv 0.27 1
rs10842705 12 26316083 intron variant A/G snv 0.20 1
rs10858966 12 90173249 intergenic variant G/C snv 0.22 1
rs10863578 1 221040655 intergenic variant G/C snv 0.74 1
rs10922502 1 88894475 upstream gene variant A/G;T snv 1
rs10931896 2 200283353 intergenic variant C/T snv 0.28 1
rs11040595 11 49857205 intron variant G/T snv 0.13 1
rs11112548 12 105478136 regulatory region variant A/T snv 3.3E-02 1
rs11117781 1 217161497 intergenic variant A/G snv 0.62 1
rs111346133 4 119996191 intergenic variant T/A;G snv 0.27 1