Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs771306418
CAMK1 ; OGG1
0.851 0.120 3 9765885 splice acceptor variant -/C delins 5
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 10
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 9
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs188096
SLC10A2
1.000 0.080 13 103052694 missense variant A/C snv 0.85 0.89 1
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs2287939
AMACR ; C1QTNF3-AMACR
0.851 0.160 5 33998778 missense variant A/C;G snv 1.6E-05; 0.70 4
rs846672 1.000 0.080 7 122990126 downstream gene variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 14
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 11
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 8
rs770649674
APC
0.807 0.120 5 112827177 missense variant A/G snv 4.0E-06 7.0E-06 6
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs1198119472
GSTA1
0.925 0.120 6 52799190 synonymous variant A/G snv 7.0E-06 2
rs1316694869
TCN2
0.925 0.160 22 30615698 missense variant A/G snv 4.0E-06 2
rs4952490
SLC8A1-AS1 ; SLC8A1
1.000 0.080 2 40145564 intron variant A/G snv 0.33 2
rs13251096 1.000 0.080 8 58505225 downstream gene variant A/G snv 0.53 1