Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2477686
PLCH2
0.807 0.040 1 2461209 intron variant G/C snv 0.64 7
rs10842262
SOX5
0.851 0.040 12 24031610 intron variant G/C snv 0.43 5
rs6080550
LOC100289473
0.851 0.040 20 1778944 intron variant C/G;T snv 9.6E-02 5
rs12870438
EPSTI1
0.925 0.040 13 42906069 intron variant G/A snv 0.27 3
rs7174015
USP8
0.925 0.040 15 50424871 intron variant G/A;T snv 3
rs10129954
DPF3
1.000 0.040 14 72683993 intron variant C/T snv 0.49 2
rs144944885
RPL23AP82 ; RABL2B
1.000 0.040 22 50776482 intron variant G/- delins 2
rs2276248
DNMT3L
1.000 0.040 21 44259375 intron variant T/C snv 6.1E-02 2
rs3819392
KIT
1.000 0.040 4 54660528 intron variant G/A snv 0.28 2
rs10841496
PDE3A
12 20368720 intron variant C/A snv 0.43 1
rs1646022
RMI2 ; LOC105371082 ; PRM2
16 11276073 intron variant C/G;T snv 0.37 1
rs2070923
LOC105371082 ; RMI2 ; PRM2
16 11275998 intron variant G/C;T snv 4.1E-06; 0.41 1
rs2282885
AHR
7 17305990 intron variant A/G snv 0.27 1
rs2301365
RMI2 ; PRM1 ; LOC105371082
16 11281429 intron variant G/T snv 0.21 1
rs2424909
DNMT3B
20 32774055 intron variant T/C snv 0.57 1
rs3817444
CLOCK
4 55509814 intron variant A/C snv 0.69 1
rs4804490
DNMT1
19 10156335 intron variant C/A snv 0.11 1
rs72609647
USP9Y ; TTTY15
Y 12678428 intron variant T/G snv 4.6E-03 1
rs724078 0.925 0.040 6 29521271 intergenic variant G/A snv 0.41 3
rs7867029
LOC107987083
0.925 0.040 9 78405502 intergenic variant G/C snv 0.22 3
rs10966811 1.000 0.040 9 25233486 intergenic variant G/A snv 0.32 2
rs1399645
LOC105373644
2 139390262 intergenic variant C/T snv 9.0E-02 1
rs6068020 20 51943113 intergenic variant T/C snv 0.63 1