Source: ALL
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: rs2607653
rs2607653
FGF14
2 1.000 0.080 13 102066314 intron variant A/G snv 5.9E-02 0.700 1.000 1 2018 2018