Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 6
rs745542298
TP73
0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs752295912
ERBB2
0.925 0.080 17 39710398 missense variant C/T snv 1.6E-05 6
rs759478535
ERBB2
0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 6
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 5
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 5
rs1114167628
PTEN
0.925 0.080 10 87961033 stop gained -/ATATCTAG delins 5
rs11544331
C7orf50 ; GPER1
0.925 0.080 7 1091775 missense variant C/T snv 0.21 0.19 5
rs13431652
SPC25
0.925 0.080 2 168896905 intron variant T/C snv 0.24 5
rs1408080623
PGR ; PGR-AS1
0.851 0.080 11 101128058 missense variant G/A snv 5
rs1462893414
ESR1
0.882 0.080 6 151944323 missense variant A/G snv 4.0E-06 7.0E-06 5
rs151322829
FAN1
0.882 0.080 15 30905792 missense variant C/G;T snv 4.2E-03 5
rs16917302
ZNF365
0.851 0.080 10 62501439 intron variant A/C snv 0.18 5
rs16940
BRCA1
0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19 5
rs17748
TREH ; PHLDB1
0.827 0.080 11 118657714 3 prime UTR variant C/T snv 0.18 5
rs1799944
BRCA2
0.882 0.080 13 32337326 missense variant A/G snv 5.4E-02 4.5E-02 5
rs180177097
PALB2
0.882 0.080 16 23635519 stop gained G/A snv 5
rs2296135
IL15RA
0.851 0.080 10 5952731 3 prime UTR variant A/C snv 0.58 5
rs28363284
RAD51D ; RAD51L3-RFFL
0.882 0.080 17 35103294 missense variant T/C snv 9.7E-03 1.1E-02 5
rs28933368
ERBB2 ; MIR4728
0.851 0.080 17 39725721 missense variant G/A snv 5
rs397509205
BRCA1
0.882 0.080 17 43070984 stop gained C/A snv 5
rs570613
GATA3
0.925 0.080 10 8064539 intron variant C/T snv 0.60 5
rs592373
LSP1
0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 5
rs778345761
PALB2
0.925 0.080 16 23614091 stop gained C/T snv 5