Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003623
ATM
0.925 0.080 11 108281855 intron variant C/G;T snv 2
rs10043985 0.925 0.080 5 111065770 upstream gene variant A/C snv 5.2E-02 2
rs1004982 0.925 0.080 15 51321614 non coding transcript exon variant T/C;G snv 2
rs10057194 0.925 0.080 5 83362752 intergenic variant A/G snv 0.16 2
rs10077427 0.925 0.080 5 75542076 intron variant A/G snv 0.13 2
rs10109984 0.925 0.080 8 47891114 intron variant T/C snv 0.54 4
rs1011329790 0.925 0.080 7 30504681 missense variant G/A snv 3
rs10145182
NIN
0.925 0.080 14 50809291 intron variant T/A;C;G snv 2
rs10169372 0.925 0.080 2 217006626 intergenic variant A/G;T snv 2
rs1017105 0.925 0.080 7 90413990 3 prime UTR variant C/T snv 0.29 2
rs1017226 0.925 0.080 5 56857565 intron variant T/C snv 5.8E-02 2
rs10175338 0.925 0.080 2 38080501 intron variant G/T snv 0.25 2
rs1020475809 0.925 0.080 16 69711027 synonymous variant A/G snv 2.0E-05 7.0E-06 2
rs10216653 0.882 0.080 8 140516886 3 prime UTR variant G/C snv 0.80 3
rs10235235 0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs10273424 0.925 0.080 7 99598450 intron variant T/A snv 0.13 3
rs1029946 0.925 0.080 7 151578720 intron variant A/G snv 0.21 2
rs1033662 0.925 0.080 20 52408842 intron variant A/G snv 0.46 2
rs1034794 0.925 0.080 7 124801348 intergenic variant A/T snv 0.69 2
rs1042638 0.925 0.080 8 80037711 3 prime UTR variant G/A;T snv 2
rs1042839
PGR
0.925 0.080 11 101051471 synonymous variant G/A snv 0.13 0.11 2
rs10439478 0.925 0.080 2 54232313 intron variant A/C;G;T snv 2
rs1044484322 0.925 0.080 2 201271565 missense variant T/A;G snv 4.0E-06 2
rs1045012 0.925 0.080 7 99386731 missense variant G/C snv 5.6E-02 7.8E-02 2
rs10463297 0.925 0.080 5 140556654 intron variant T/C snv 0.29 2