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: rs448792
rs448792
FRY
2 1.000 0.080 13 32103287 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs543554
rs543554
FRY
2 1.000 0.080 13 32127501 intron variant A/G;T snv 0.700 1.000 1 2017 2017