Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3211770
F10
13 113139535 intron variant G/A snv 0.11 2
rs776905
F10
13 113127628 intron variant A/C snv 8.7E-02 2
rs2026160
F10
13 113138579 intron variant C/A snv 0.69 1
rs474810
F10
13 113126596 intron variant T/C snv 0.14 1
rs556694
F10
13 113125727 intron variant T/C snv 0.17 1
rs776906
F10-AS1 ; F10
13 113130274 non coding transcript exon variant A/C;G snv 1
rs2480946
F10 ; F10-AS1
13 113130406 intron variant A/G snv 0.13 1