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: rs121908669
rs121908669
LRP5
1 1.000 0.040 11 68357672 missense variant G/C snv 0.800 1.000 1 2003 2003
dbSNP: rs121908670
rs121908670
LRP5
3 0.882 0.080 11 68363784 missense variant G/A snv 0.800 1.000 1 2003 2003
dbSNP: rs121908673
rs121908673
LRP5
2 0.925 0.160 11 68363818 missense variant C/T snv 0.800 1.000 1 2003 2003
dbSNP: rs121908671
rs121908671
LRP5
4 0.851 0.120 11 68357801 missense variant G/A snv 0.700 0