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: rs1352056360
rs1352056360
LCAT
2 0.925 0.080 16 67940467 missense variant C/G snv 1.2E-05 0.010 1.000 1 1998 1998