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: rs121908668
rs121908668
LRP5
5 0.882 0.240 11 68357673 missense variant G/T snv 0.700 1.000 5 2002 2007
dbSNP: rs1085307078
rs1085307078
LRP5
1 11 68357754 missense variant A/G snv 0.700 1.000 2 2004 2006