Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070565
DNMT3L
0.925 0.080 21 44261270 splice region variant T/C snv 0.70 0.75 3
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs6523
INSL3
0.882 0.200 19 17821329 missense variant T/C snv 0.65 0.70 4
rs3817444
CLOCK
4 55509814 intron variant A/C snv 0.69 1
rs2477686
PLCH2
0.807 0.040 1 2461209 intron variant G/C snv 0.64 7
rs6068020 20 51943113 intergenic variant T/C snv 0.63 1
rs2631367
MIR3936HG ; SLC22A5
0.925 0.120 5 132369766 5 prime UTR variant C/G snv 0.59 4
rs4045481
RNF212
1.000 0.040 4 1096837 stop gained G/A snv 0.64 0.57 2
rs2424909
DNMT3B
20 32774055 intron variant T/C snv 0.57 1
rs6166
FSHR
0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 17
rs6476866 9 4459274 intergenic variant G/A snv 0.55 1
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs10129954
DPF3
1.000 0.040 14 72683993 intron variant C/T snv 0.49 2
rs8069533
YBX2
17 7294314 missense variant A/G snv 0.46 0.48 1
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs12348
TUSC1
0.925 0.040 9 25677217 3 prime UTR variant T/C snv 0.44 3
rs10842262
SOX5
0.851 0.040 12 24031610 intron variant G/C snv 0.43 5
rs10841496
PDE3A
12 20368720 intron variant C/A snv 0.43 1
rs175080
MLH3
0.776 0.240 14 75047125 missense variant G/A snv 0.40 0.43 9
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs724078 0.925 0.040 6 29521271 intergenic variant G/A snv 0.41 3