Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 5
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1049253
CASP3
0.851 0.160 4 184627797 3 prime UTR variant A/G snv 0.13 4
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 9
rs1058172
CYP2D6 ; NDUFA6-DT
0.882 0.080 22 42127526 missense variant C/G;T snv 4.4E-06; 9.2E-02 2
rs10877887
LINC01465 ; MIRLET7I
0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs10882272
FFAR4
0.925 0.040 10 93588425 3 prime UTR variant T/C snv 0.44 2
rs10950641
SNX8
0.925 0.040 7 2294751 intron variant G/A snv 2.9E-02 3
rs11016879
MGMT
0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1138272
GSTP1
0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11515
CDKN2A ; CDKN2A-DT
0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88 6
rs11540483
TAX1BP1
0.925 0.040 7 27787484 missense variant T/A snv 8.2E-02 7.7E-02 2
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs11752942
LINC00951 ; TDRG1
0.882 0.080 6 40354019 intron variant A/G snv 0.46 3
rs1183646267
ATM
0.925 0.040 11 108281026 missense variant A/G snv 2
rs1208
NAT2
0.807 0.080 8 18400806 missense variant G/A;T snv 0.62; 4.0E-06 8
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62