Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs4978754
ELP1
0.851 0.080 9 108884801 intron variant T/C snv 0.92 4
rs4645878
BAX
0.882 0.120 19 48954681 upstream gene variant A/G snv 0.89 5
rs784621
HEYL
1.000 0.080 1 39641113 upstream gene variant T/C snv 0.85 1
rs2966952
FASTKD3 ; MTRR
1.000 0.080 5 7867917 missense variant T/C;G snv 0.82; 4.0E-06 0.85 1
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 10
rs344781
PLAUR
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs959173
CAV1
0.925 0.120 7 116542000 intron variant C/T snv 0.78 2
rs586339
KDM4A
1.000 0.080 1 43671586 missense variant C/A;G;T snv 0.70 0.78 2
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs7372209
CTDSPL ; MIR26A1
0.807 0.160 3 37969217 intron variant T/C snv 0.77 7
rs751402
ERCC5 ; BIVM-ERCC5
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs6759180
RRM2
1.000 0.080 2 10126436 intron variant G/A snv 0.74 1
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs5753025
HORMAD2
1.000 0.080 22 30146168 intron variant T/C snv 0.71 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2725264
ABCG2
1.000 0.080 4 88104957 intron variant C/T snv 0.70 1
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 3
rs373572
RAD18
0.882 0.120 3 8913705 missense variant C/T snv 0.68 0.70 6
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs228729
PER3
0.827 0.120 1 7785635 intron variant T/C snv 0.69 0.69 5
rs12614710
EPAS1
1.000 0.080 2 46337952 intron variant T/G snv 0.69 1