Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs1316694869
TCN2
0.925 0.160 22 30615698 missense variant A/G snv 4.0E-06 2
rs927650
CYP24A1
0.763 0.240 20 54156202 intron variant T/A;C snv 9
rs4813802 0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28 2
rs35051736
CYP24A1
1.000 0.080 20 54171650 missense variant C/G;T snv 4.0E-06; 3.0E-03 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 38
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 18
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 17
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 8
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 4
rs1319831679
NQO1
1.000 0.080 16 69711169 missense variant C/T snv 4.0E-06 7.0E-06 1