Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6045400
DZANK1
20 18441344 intron variant A/G snv 0.72 1
rs10789181
DNAJC6
1 65350884 intron variant A/G snv 0.72 1
rs1532331
ZNF131
5 43116728 intron variant G/T snv 0.70 1
rs7028185 9 117897330 intron variant A/G snv 0.69 1
rs28672845 3 88221477 regulatory region variant A/C snv 0.69 1
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 4
rs7766336
LIN28B-AS1 ; LIN28B
6 104940530 intron variant T/G snv 0.69 1
rs11125803
ADCY3
2 24829308 intron variant C/T snv 0.68 1
rs8087694 18 64672065 intergenic variant G/C;T snv 0.68 1
rs2378662
LOC101927575
9 84092374 intron variant G/A snv 0.67 1
rs9640621 7 94464841 intergenic variant C/T snv 0.67 1
rs7853970 9 84100651 downstream gene variant T/C snv 0.66 1
rs6563739
MIR4305 ; COG6
13 39665648 intron variant G/T snv 0.66 1
rs11022756
ARNTL
11 13293892 intron variant A/C snv 0.65 1
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs6762477
RBM6
3 50055776 intron variant G/A snv 0.64 1
rs314273
LIN28B
6 105014007 intron variant T/G snv 0.64 1
rs10780649
LOC101927575
9 84088646 intron variant T/G snv 0.64 2
rs7438414
HPGDS
4 94344671 upstream gene variant T/C snv 0.64 1
rs167539
LIN28B
6 104962173 intron variant C/A snv 0.64 1
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 3
rs12607903
DLGAP1
18 3817134 intron variant C/T snv 0.64 1
rs6499244
NFAT5
1.000 0.040 16 69701368 3 prime UTR variant T/A snv 0.64 2
rs10870546
MUC8
12 132478023 intergenic variant A/G snv 0.63 1
rs2688325
CSMD1
8 3909688 intron variant T/C snv 0.63 1