Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1056629
MPHOSPH6
0.827 0.120 16 82148499 3 prime UTR variant T/C snv 0.14 6
rs60745952
LOC107986195 ; LOC105377481
0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs730882002
TP53
0.925 0.040 17 7674956 missense variant T/C snv 6
rs10817938
PTCSC2
0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
rs1487151044
ZEB1
0.851 0.080 10 31510817 missense variant T/C snv 5
rs4647958
SNAI1
0.851 0.080 20 49984094 missense variant T/C snv 0.18 0.29 5
rs867114783
TP53
17 7675109 missense variant T/C snv 5
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 4
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 4
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs1219211410
CDC25B
0.925 0.080 20 3800494 missense variant T/C snv 3
rs200081710
TNIP3
1.000 0.120 4 121154648 missense variant T/C snv 7.0E-06 3
rs7371084
GTF2A1L ; LHCGR ; STON1-GTF2A1L
0.925 0.120 2 48712814 intron variant T/C snv 0.12 3
rs140451238
ITK
1.000 0.080 5 157208978 synonymous variant T/C snv 1.6E-04 7.8E-04 2
rs148626207
NFKB1 ; LOC105377347
4 102612593 missense variant T/C snv 8.0E-06 1.4E-05 1
rs2375801
MTNR1A
4 186550471 intron variant T/C snv 0.34 1
rs2994809
REG4
1 119809354 intron variant T/C snv 0.91 1
rs3206652
CD47
3 108046402 3 prime UTR variant T/C snv 0.27 1
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs3809865
THCAT158 ; ITGB3
0.790 0.240 17 47311220 3 prime UTR variant T/A;G snv 11
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 21
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 17
rs121913492
GNAQ
0.790 0.160 9 77794572 missense variant T/A;C;G snv 11