Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 5
rs498136 0.851 0.080 11 69552350 intergenic variant A/C snv 0.68 4
rs10816595 0.851 0.080 9 107947454 regulatory region variant A/G snv 0.33 3
rs2111398 0.882 0.080 12 12922268 downstream gene variant A/G snv 0.49 3
rs2695237 0.882 0.080 1 226415934 upstream gene variant T/A;C snv 3
rs7041168 0.882 0.080 9 107936435 intergenic variant G/A;T snv 3
rs75691080 0.882 0.080 20 63638397 downstream gene variant C/T snv 9.1E-02 3
rs1636744
AHR
0.851 0.080 7 16944656 intron variant C/T snv 0.31 4
rs1057519786
ARAF
0.882 0.160 X 47566722 missense variant C/G;T snv 3
rs1057519876
ARAF
0.882 0.160 X 47566721 missense variant T/G snv 3
rs72704658
ARNT
0.882 0.080 1 150860534 intron variant T/C snv 0.33 3
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 6