Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1321845532
TP53
0.851 0.160 17 7670685 frameshift variant GG/A;G delins 4
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs56307747
ELN ; ELN-AS1
0.776 0.160 7 74059952 missense variant G/A;C snv 4.0E-06 8
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs764918809
MDM2
0.827 0.160 12 68839337 missense variant T/C snv 4.0E-06 6
rs121964872
CDH1
0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 3
rs61755649
RAD51B
0.882 0.160 14 67885891 missense variant C/T snv 6.8E-05 4.9E-05 3
rs495139
ENOSF1
0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs755378873
SLC13A5
0.851 0.120 17 6694197 missense variant C/A;T snv 4.0E-06 5
rs2240308
AXIN2
0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs3923087
AXIN2
0.827 0.160 17 65553143 intron variant T/C snv 0.58 5
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs3020450
ESR2
0.807 0.200 14 64301584 splice region variant C/A;T snv 10
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs7937840
INCENP
0.807 0.200 11 62126500 intron variant C/T snv 0.20 7
rs12451939
MED13
1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 1
rs12938171
INTS2
1.000 0.120 17 61902994 intron variant G/A snv 9.0E-03 1
rs12937080
BRIP1
1.000 0.120 17 61852376 intron variant A/G;T snv 1
rs4988344
BRIP1
0.882 0.120 17 61847251 intron variant G/C snv 0.20 0.15 4
rs34289250
BRIP1
0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 2
rs1064795649
BRIP1
1.000 0.120 17 61799205 frameshift variant CT/- delins 2
rs2191249
BRIP1
0.882 0.120 17 61758503 intron variant T/G snv 0.79 3