Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1303
SERPINA1
0.925 0.040 14 94378506 missense variant T/G snv 0.28 0.22 4
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs2390582
LOC105378851
1 90478350 intergenic variant A/G snv 0.15 1
rs1440581
PPM1K-DT
1.000 0.080 4 88305270 intron variant T/A;C snv 4
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs113805659
MAGI2
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs2168889 4 74357994 intergenic variant A/G snv 4.7E-02 1
rs16850360 4 74006728 intron variant A/G snv 4.2E-02 2
rs12507628 4 72779634 regulatory region variant G/A snv 0.13 1
rs10500569
LOC107984814
16 72722202 intron variant G/A;C;T snv 1
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 6
rs1851024 4 71842104 intergenic variant G/A snv 0.93 1
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 3
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 4
rs741013
PRICKLE2
3 64306961 intron variant A/T snv 6.0E-02 1
rs17404667
PRICKLE2
3 64288876 intron variant C/G snv 6.2E-02 1
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs2306786
MYO1E
15 59195731 intron variant C/G snv 8.0E-02 1
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs16939881
ALDH1A2 ; AQP9
15 58179780 intron variant G/C;T snv 2
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11