Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 4
rs974120 0.851 0.200 8 2789080 intron variant T/C;G snv 4
rs1555902 1.000 0.160 13 108204435 downstream gene variant C/A snv 0.10 1
rs193451 1.000 0.160 7 108670542 intergenic variant A/G snv 0.36 1
rs79480871 0.925 0.160 2 24471603 intergenic variant C/T snv 9.3E-02 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs4148388
ABCC2
1.000 0.160 10 99790008 intron variant G/A;C snv 1
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 54
rs2231137
ABCG2
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 12
rs764931115
AKT1
0.925 0.200 14 104780148 missense variant T/C snv 4.0E-06 3
rs1450703683
ANOS1
1.000 0.160 X 8533018 missense variant T/C snv 1.9E-05 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 264
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 14
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 11
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 7
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 2
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 1
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 1
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29