Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs474671
rs474671
F10
1 13 113121904 upstream gene variant T/C snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs776905
rs776905
F10
2 13 113127628 intron variant A/C snv 8.7E-02 0.700 1.000 1 2017 2017