Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752106647
FN1
1.000 0.080 2 215406406 missense variant C/T snv 8.0E-06 1
rs1373375768
FN1
1.000 0.080 2 215361578 missense variant C/T snv 4.0E-06 1
rs1553659131
FN1
0.925 0.160 2 215428306 missense variant A/C snv 1
rs1553667072
FN1
0.882 0.200 2 215433372 missense variant A/G snv 1
rs1553658926
FN1
0.925 0.160 2 215428246 missense variant A/C snv 1
rs137854488
FN1
1.000 0.120 2 215406306 missense variant T/C snv 1
rs1553669703
FN1 ; LOC105373868
0.925 0.160 2 215434713 missense variant C/A snv 1
rs137854486
FN1 ; LOC112268430
1.000 0.120 2 215376612 missense variant A/T snv 1
rs137854487
LOC112268430 ; FN1
1.000 0.120 2 215375685 missense variant A/C;G snv 1