Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2410373 0.851 0.120 8 16066997 intergenic variant A/C snv 0.34 6
rs16917302
ZNF365
0.851 0.080 10 62501439 intron variant A/C snv 0.18 5
rs190900046
BRCA1
0.827 0.160 17 43104197 synonymous variant A/C snv 8.0E-06 4.2E-05 5
rs6180
GHR
0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 5
rs833052 0.827 0.160 6 43755598 intergenic variant A/C snv 0.88 5
rs11895168
ERBB4
0.925 0.080 2 211377467 3 prime UTR variant A/C snv 0.68 4
rs2296135
IL15RA
0.851 0.080 10 5952731 3 prime UTR variant A/C snv 0.58 4
rs3864659
AGO2
0.925 0.080 8 140545763 intron variant A/C snv 0.16 4
rs4987208
RAD52
0.851 0.160 12 913403 stop gained A/C snv 3.5E-02 2.1E-02 4
rs7713645
PIK3R1
0.851 0.200 5 68231498 intron variant A/C snv 0.58 4
rs8004379
NPAS3
0.851 0.120 14 33599495 intron variant A/C snv 0.12 4
rs981782
HCN1
0.851 0.080 5 45285616 intron variant A/C snv 0.34 4
rs985325188
APEX1 ; OSGEP
0.851 0.080 14 20456806 missense variant A/C snv 4
rs13423759
ERBB4
0.925 0.080 2 211381247 3 prime UTR variant A/C snv 6.8E-02 3
rs15869
BRCA2
0.925 0.080 13 32398875 3 prime UTR variant A/C snv 0.15 3
rs2071002
NQO2-AS1 ; NQO2
0.882 0.080 6 3000069 5 prime UTR variant A/C snv 0.32 3
rs2787486
STXBP4
0.925 0.080 17 55132413 intron variant A/C snv 0.33 3
rs34434221
AKAP13
0.882 0.080 15 85579644 missense variant A/C snv 2.2E-02 2.2E-02 3
rs406113
GPX6
0.882 0.160 6 28515705 missense variant A/C snv 0.38 0.45 3
rs7719521
SPARC
0.882 0.120 5 151669843 intron variant A/C snv 0.65 3
rs10043985 0.925 0.080 5 111065770 upstream gene variant A/C snv 5.2E-02 2
rs11085735
KEAP1
0.925 0.080 19 10491504 intron variant A/C snv 0.92 2
rs12239582
ST6GALNAC3
0.925 0.080 1 76371552 intron variant A/C snv 0.30 2
rs1326306 0.925 0.080 13 31364049 intergenic variant A/C snv 0.67 2
rs1482057
RORA
0.925 0.080 15 60772552 intron variant A/C snv 0.80 2