Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 6
rs1017621656
TGFB1
0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05 3
rs10222633
CASR
0.925 0.080 3 122258079 intron variant G/A snv 0.45 2
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 1
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 22
rs1042821
MSH6
0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs10450310
MBL2
0.925 0.080 10 52764898 downstream gene variant G/A snv 0.29 2
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 8
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 42
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 8
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519725
KRAS
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 4
rs1057519822
MAP2K1
0.925 0.080 15 66481818 missense variant T/A snv 2
rs1060503118
PMS2
0.925 0.080 7 5987422 missense variant C/T snv 2
rs1064795841
TP53
0.882 0.080 17 7674971 missense variant C/T snv 4
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 32
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15