Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs142252570 14 97296313 intergenic variant TTAA/- delins 4.0E-02 1
rs11285463
LIN28B
6 104944130 intron variant TT/-;T;TTT delins 1
rs35020808
LOC105373831
2 198743564 intron variant TT/-;T;TTT delins 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs10780649
LOC101927575
9 84088646 intron variant T/G snv 0.64 2
rs35436838
RORB
9 74658994 intron variant T/G snv 9.8E-02 2
rs80170948
SREK1IP1
5 64724489 missense variant T/G snv 3.0E-02 2.8E-02 2
rs10007754
TACR3
4 103706285 intron variant T/G snv 0.34 1
rs10816359
LINC01505
9 105995389 intron variant T/G snv 0.18 1
rs11039266
CELF1
11 47510843 intron variant T/G snv 0.20 1
rs12476703 2 199254540 intergenic variant T/G snv 0.54 1
rs314273
LIN28B
6 105014007 intron variant T/G snv 0.64 1
rs35184820
LINC00649
21 33948637 intron variant T/G snv 0.45 1
rs35413307 13 111539431 intergenic variant T/G snv 0.57 1
rs4365199 14 60527495 intron variant T/G snv 0.62 1
rs4369815 2 156270452 intergenic variant T/G snv 4.5E-02 1
rs480263
LOC105375951
9 1709382 regulatory region variant T/G snv 0.76 1
rs62009090 15 77544713 intergenic variant T/G snv 0.62 1
rs73204208
CHAF1B
21 36419168 downstream gene variant T/G snv 0.10 1
rs7766336
LIN28B-AS1 ; LIN28B
6 104940530 intron variant T/G snv 0.69 1
rs9795476
SIRT3 ; PSMD13
11 235894 intron variant T/G snv 0.79 1
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 7
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv 5
rs4549631 6 126645162 intron variant T/C;G snv 3