Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 18
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 16
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 16
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 15
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 15
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 14
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 13
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 13