Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 18
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 18
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 16
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs149617956
MITF
0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 12
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519929
PIK3CA
0.776 0.320 3 179199066 missense variant G/A snv 10
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 10
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 9
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 9
rs587777894
MTOR
0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 7
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7