Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12894364 1.000 0.080 14 37588860 downstream gene variant C/T snv 7.6E-02 1
rs2294750 1.000 0.080 1 10824979 regulatory region variant G/A snv 0.10 1
rs2477137 1.000 0.080 1 17304110 upstream gene variant G/T snv 0.20 1
rs2844695 1.000 0.080 6 30968237 intergenic variant T/C snv 0.28 1
rs2904268 1.000 0.080 20 50433551 upstream gene variant C/A;G snv 1
rs35399661 1.000 0.080 6 32623213 upstream gene variant T/C snv 0.16 1
rs3763338 1.000 0.080 6 28926534 upstream gene variant G/A snv 0.11 1
rs6854472 1.000 0.080 4 89513521 intron variant G/T snv 0.30 1
rs1789903
ADH1C ; ADH1B
1.000 0.080 4 99340884 intron variant C/A;G snv 1
rs764058037
AKT2
1.000 0.080 19 40241984 missense variant C/A;T snv 1.2E-05; 8.0E-06 1
rs1322178
ATG5
1.000 0.080 6 106183905 intron variant C/T snv 0.15 1
rs671116
ATG5
1.000 0.080 6 106312722 intron variant A/G snv 0.41 1
rs1642764
ATP1B2
1.000 0.080 17 7654516 intron variant C/T snv 0.45 1
rs1009316
BAX
1.000 0.080 19 48955313 non coding transcript exon variant T/C;G snv 1
rs61271866
CDKN2B-AS1 ; CDKN2A
1.000 0.080 9 21997016 intron variant T/A snv 0.19 1
rs1033667
CHEK2
1.000 0.080 22 28734312 intron variant C/T snv 0.30 1
rs2396092
CUL3
1.000 0.080 2 224470573 3 prime UTR variant A/G snv 0.18 1
rs3138373
EFCAB12
1.000 0.080 3 129430178 upstream gene variant T/C snv 0.13 1
rs1618536
ERCC2
1.000 0.080 19 45368348 intron variant T/A;C snv 1
rs10138277
HEATR5A
1.000 0.080 14 31393927 intron variant T/A;C snv 1
rs6683039
IL23R ; C1orf141
1.000 0.080 1 67165650 intron variant C/T snv 0.47 1
rs12188136
LINC01411
1.000 0.080 5 174407635 intron variant A/G snv 0.30 1
rs2866943
LOC101927182 ; PTPRT
1.000 0.080 20 42079239 3 prime UTR variant C/T snv 0.20 1
rs6029959
LOC101927182 ; PTPRT
1.000 0.080 20 42076024 3 prime UTR variant C/A;T snv 1
rs1206093523
LOC105377015 ; TGFBR2
1.000 0.080 3 30606915 missense variant C/T snv 9.2E-06 1