Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7325927
FAM155A-IT1 ; FAM155A
0.925 0.040 13 107823165 intron variant C/T snv 0.38 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs660118
SART1
0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 6
rs11860248
RBBP6
0.882 0.040 16 24566445 intron variant T/G snv 0.27 5
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1957106
NFKBIA
0.851 0.040 14 35404564 synonymous variant G/A snv 0.28 0.25 4
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs9642393
EGFR
0.925 0.040 7 55177954 intron variant T/C snv 0.24 2
rs2017309
CHEK2
0.851 0.040 22 28735438 intron variant T/A snv 0.23 4
rs1800734
EPM2AIP1 ; MLH1
0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs3851634
POLR3B
0.882 0.040 12 106419124 intron variant T/C snv 0.22 4
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs7732320
SSBP2
0.925 0.040 5 81423306 intron variant C/T snv 0.22 2
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs17748
TREH ; PHLDB1
0.827 0.080 11 118657714 3 prime UTR variant C/T snv 0.18 5
rs6470745
CCDC26
0.882 0.040 8 129629675 intron variant A/G snv 0.18 3
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5