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: rs74652506
rs74652506
1 1.000 0.040 3 43402386 intron variant C/T snv 9.7E-02 0.700 1.000 1 2019 2019