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: rs377258285
rs377258285
LRP5
1 1.000 0.120 11 68425202 missense variant C/T snv 5.6E-05 6.3E-05 0.700 1.000 5 2001 2008