Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15 13
rs4986764
BRIP1
0.827 0.120 17 61685986 missense variant A/G snv 0.60 0.61 8
rs137852986
BRIP1
0.732 0.440 17 61716051 stop gained G/A snv 1.7E-04 1.5E-04 5
rs2048718
BRIP1
0.827 0.120 17 61863458 5 prime UTR variant C/T snv 0.42 5
rs11871753
BRIP1
0.851 0.120 17 61779284 intron variant A/G snv 0.75 4
rs16945628
BRIP1
0.851 0.120 17 61789868 intron variant T/C snv 0.60 4
rs7220719
BRIP1
0.882 0.120 17 61736921 intron variant A/G snv 0.73 3
rs4988349
BRIP1
0.925 0.080 17 61784279 missense variant T/A snv 3.6E-05 2.8E-05 2
rs769797684
BRIP1
0.925 0.080 17 61744510 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 2