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: rs2306272
rs2306272
LRIG1 ; SLC25A26
2 1.000 0.080 3 66384219 missense variant T/C snv 0.31 0.25 0.700 1.000 1 2018 2018