Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2269700
DELEC1
9 115401284 non coding transcript exon variant C/T snv 0.67 0.71 1
rs4646
MIR4713HG ; CYP19A1
0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs4562
ELP5 ; CLDN7
0.925 0.080 17 7260420 missense variant A/G snv 0.65 0.70 3
rs3213245
XRCC1 ; PINLYP
0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13
rs1332018
GSTM5 ; GSTM3
0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs4986764
BRIP1
0.827 0.120 17 61685986 missense variant A/G snv 0.60 0.61 8
rs735943
EXO1
1 241866849 missense variant A/G snv 0.60 0.59 1
rs1864182
ATG10
0.827 0.120 5 82253421 missense variant C/A;G snv 0.59 0.47 6
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 16
rs9856
XIAP
0.925 0.120 X 123911791 3 prime UTR variant C/T snv 0.57 4
rs7439366
UGT2B7
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs13332
CTSB
0.925 0.120 8 11849072 synonymous variant T/C;G snv 3.5E-02; 0.56 6
rs605059
HSD17B1 ; LOC108783654
0.763 0.160 17 42554888 missense variant G/A;C;T snv 0.56; 9.0E-05; 1.4E-05 15
rs9862
TIMP3 ; SYN3
1.000 0.080 22 32857293 missense variant T/A;C snv 4.0E-06; 0.55 3
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs2536512
SOD3
0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs2227928
ATR
0.851 0.200 3 142562770 missense variant A/G snv 0.55 0.63 5
rs169068
SSTR5-AS1 ; SSTR5
0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs627928
RNASEL
0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10