Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7697932
H2AZ1-DT
1.000 0.120 4 100084161 intron variant A/G snv 0.72 1
rs4804368
INSR
1.000 0.120 19 7190279 intron variant A/G;T snv 1
rs234043
LINC02068
1.000 0.120 3 172595577 non coding transcript exon variant T/C snv 0.74 1
rs11637556
MAP2K1
1.000 0.120 15 66436613 intron variant A/C;G snv 1
rs4662750
MYO7B
1.000 0.120 2 127634972 non coding transcript exon variant A/C snv 0.69 1
rs10054504
PDZD2
1.000 0.120 5 32000377 intron variant T/A;C snv 1
rs59294613
POT1
1.000 0.120 7 124914213 intron variant C/A snv 0.28 1
rs35252396
PVT1
1.000 0.120 8 127877125 intron variant AC/CG mnv 1
rs6470588
PVT1
1.000 0.120 8 127877125 intron variant A/C snv 0.53 1
rs6470589
PVT1
1.000 0.120 8 127877126 intron variant C/A;G snv 1
rs10484683
SAMD5
1.000 0.120 6 147830941 intron variant A/G snv 0.18 1
rs13027293
STEAP3
1.000 0.120 2 119243542 intron variant G/T snv 0.33 1
rs2203002
TFDP2
1.000 0.120 3 142077397 intron variant C/T snv 6.4E-02 1
rs12105521
ZEB2
1.000 0.120 2 144450769 intron variant G/A;T snv 1
rs12105918
ZEB2
1.000 0.120 2 144450626 intron variant T/C snv 6.1E-02 1
rs13401103
ZEB2
1.000 0.120 2 144441056 intron variant G/A;T snv 1
rs72858474
ZEB2
1.000 0.120 2 144441322 intron variant G/A snv 6.2E-02 1
rs72858496
ZEB2
1.000 0.120 2 144452349 intron variant C/T snv 5.9E-02 1
rs11813268 0.925 0.120 10 103922538 upstream gene variant C/T snv 0.31 2
rs1417080 0.925 0.120 9 79515946 non coding transcript exon variant T/C snv 0.35 2
rs3118523 0.925 0.120 9 134443675 downstream gene variant G/A snv 0.75 2
rs6466135 0.925 0.120 7 106861053 upstream gene variant A/G snv 0.71 2
rs7132434 0.925 0.120 12 26319629 non coding transcript exon variant A/G snv 0.62 2
rs748964 0.925 0.120 9 134442243 downstream gene variant C/G;T snv 2
rs1154454
ADH7
0.925 0.120 4 99417185 intron variant A/G snv 0.22 2