Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6577555
MIR34AHG ; MIR34A
1.000 0.080 1 9152228 intron variant A/C snv 0.74 1
rs12128240
MIR34AHG ; MIR34A
1.000 0.080 1 9151244 non coding transcript exon variant C/G;T snv 1
rs4932370 1.000 0.080 15 90861475 intergenic variant G/A;C snv 2
rs3179089
CALM1
1.000 0.080 14 90407068 3 prime UTR variant C/G snv 0.39 1
rs982873 0.925 0.160 13 90145678 intergenic variant T/C snv 0.65 2
rs9301654 1.000 0.080 13 90142152 intergenic variant A/G snv 0.20 1
rs1491034 1.000 0.080 13 90049366 intergenic variant A/G snv 0.17 1
rs11018628
NOX4
1.000 0.080 11 89473343 intron variant T/C;G snv 2
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs60942712 0.882 0.120 3 88998609 intergenic variant G/T snv 7.9E-02 5
rs1049255
CYBA
0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs2231137
ABCG2
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 13
rs12445022 1.000 0.080 16 87541726 intergenic variant G/A snv 0.27 2
rs4148738
ABCB1
0.925 0.120 7 87533733 intron variant C/T snv 0.62 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs34354898 1.000 0.080 6 87129144 intergenic variant G/A;T snv 1
rs12438353
AGBL1
1.000 0.080 15 86771849 intron variant C/T snv 0.38 1
rs7202008
ZDHHC7
1.000 0.080 16 84985897 intron variant A/C snv 1.2E-02 1
rs11498973 1.000 0.080 10 84732025 intergenic variant A/C snv 0.19 1
rs10400694 1.000 0.080 14 84147550 intergenic variant G/C;T snv 1
rs7193788 0.925 0.120 16 82622555 upstream gene variant A/G snv 0.16 4
rs1864169
GTF2A1 ; SNORA79
0.851 0.200 14 81203689 intron variant G/T snv 0.78 5
rs2682818
MIR618 ; LOC105369869 ; LIN7A
0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14