Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41293497
BRCA2
0.724 0.440 13 32340037 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 14
rs147187700
C11orf65 ; ATM
0.925 0.120 11 108310218 missense variant G/C snv 1.3E-04 1.8E-04 3
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 3