Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1564919048
FGFR2
0.732 0.280 10 121520106 missense variant C/A snv 23
rs1559662068
BRPF1
0.925 3 9741340 frameshift variant AG/T delins 10