Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909641
FGFR1
0.763 0.520 8 38419720 missense variant G/A snv 9
rs779707422
FGFR1
0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 7
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 7
rs121917759
HRAS ; LRRC56
0.790 0.480 11 533466 missense variant G/A snv 7
rs1057519725
KRAS
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 2