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: rs104893848
rs104893848
LRAT
2 0.925 0.080 4 154744851 missense variant T/A;C snv 5.6E-05 0.700 1.000 3 2001 2007
dbSNP: rs1560870755
rs1560870755
LRAT
2 0.925 0.080 4 154744543 frameshift variant AT/- del 0.700 0