Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 1
rs137852564
AR
0.827 0.240 X 67722976 missense variant G/A;T snv 1
rs137852567
AR
0.882 0.200 X 67717595 missense variant A/G snv 1
rs80358972
BRCA2
0.742 0.480 13 32356472 stop gained C/A;T snv 8.0E-06; 3.2E-05 1
rs10808556
CASC8 ; POU5F1B ; PCAT1 ; CCAT2
0.925 0.080 8 127400902 non coding transcript exon variant C/T snv 0.50 1
rs130067
CCHCR1
0.851 0.200 6 31150734 missense variant T/G snv 0.23 0.21 1
rs2659056
LOC105372441 ; KLK15
0.925 0.080 19 50832687 intron variant T/C snv 0.21 1
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 1
rs9623117
TNRC6B
0.851 0.200 22 40056115 intron variant T/C snv 0.38 1
rs10749408 0.925 0.080 10 121208012 intergenic variant C/T snv 0.72 2
rs10788165 0.925 0.080 10 121284700 regulatory region variant T/G snv 0.35 2
rs10895304 0.925 0.080 11 102519261 downstream gene variant A/G snv 0.20 2
rs10920531 0.925 0.080 1 202939708 downstream gene variant A/C snv 0.57 2
rs11067228 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 2
rs11079344 0.925 0.080 17 58297122 downstream gene variant A/G snv 0.14 2
rs1125927 0.925 0.080 13 62947758 intergenic variant G/A snv 9.2E-02 2
rs11986220 0.925 0.080 8 127519444 intergenic variant A/G;T snv 2
rs12277366 0.925 0.080 11 76639075 intergenic variant G/A;C snv 2
rs12315175 0.925 0.080 12 107105494 intron variant T/C snv 0.18 2
rs12680047 0.925 0.080 8 127746615 downstream gene variant T/C snv 0.49 2
rs12723593 0.925 0.080 1 182569447 downstream gene variant C/G snv 0.30 2
rs13083990 0.925 0.080 3 122295719 downstream gene variant T/C snv 0.30 2
rs1429409 0.925 0.080 2 16227278 non coding transcript exon variant C/A;T snv 4.4E-02 2
rs156113 0.925 0.080 6 104369868 intergenic variant A/T snv 0.96 2
rs16844874 0.925 0.080 2 210737692 intergenic variant T/C snv 0.16 2