List of variants in gene LRP5 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_002335.4(LRP5):c.4000+9C>T	rs148685646	0.00389
NM_002335.4(LRP5):c.4049T>G (p.Leu1350Arg)	rs531205284	0.00018
NM_002335.4(LRP5):c.1199C>T (p.Ala400Val)	rs201320326	0.00014
NM_002335.4(LRP5):c.3245A>G (p.Tyr1082Cys)	rs113804402	0.00011
NM_002335.4(LRP5):c.1226C>T (p.Thr409Met)	rs199686378	0.00004
NM_002335.4(LRP5):c.1519G>A (p.Gly507Ser)	rs765290711	0.00002
NM_002335.4(LRP5):c.98C>T (p.Pro33Leu)	rs753259758	0.00001
NM_002335.4(LRP5):c.169A>G (p.Ile57Val)
NM_002335.4(LRP5):c.35T>A (p.Leu12Gln)	rs1019409513
NM_002335.4(LRP5):c.796C>T (p.Arg266Cys)
NM_002335.4(LRP5):c.893G>A (p.Arg298His)

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