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: rs121908674
rs121908674
LRP5
3 0.882 0.160 11 68410076 missense variant C/G;T snv 0.700 0
dbSNP: rs28939709
rs28939709
LRP5
2 0.925 0.080 11 68436987 missense variant G/A snv 8.0E-06 0.700 0
dbSNP: rs80358307
rs80358307
LRP5
1 1.000 11 68363862 frameshift variant GGGGAAGAGG/- delins 0.700 0
dbSNP: rs80358312
rs80358312
LRP5
4 0.925 0.080 11 68403607 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs80358313
rs80358313
LRP5
3 0.882 0.160 11 68406550 missense variant G/A;C;T snv 1.2E-05; 1.2E-05; 3.2E-05 0.700 0