List of variants in gene LRP5 reported as benign by PreventionGenetics, part of Exact Sciences

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002335.4(LRP5):c.1647T>C (p.Phe549=)	rs545382	0.83202
NM_002335.4(LRP5):c.3357G>A (p.Val1119=)	rs556442	0.55735
NM_002335.4(LRP5):c.884-4T>C	rs314776	0.48379
NM_002335.4(LRP5):c.1412+8G>A	rs4988319	0.15090
NM_002335.4(LRP5):c.2220C>T (p.Asn740=)	rs2306862	0.11683
NM_002335.4(LRP5):c.3989C>T (p.Ala1330Val)	rs3736228	0.10701
NM_002335.4(LRP5):c.2318+6T>C	rs4988322	0.06393
NM_002335.4(LRP5):c.1932G>A (p.Glu644=)	rs2277268	0.06342
NM_002335.4(LRP5):c.3297C>T (p.Asp1099=)	rs17149104	0.02225
NM_002335.4(LRP5):c.4788C>T (p.Thr1596=)	rs113442867	0.01233
NM_002335.4(LRP5):c.266A>G (p.Gln89Arg)	rs41494349	0.00826
NM_002335.4(LRP5):c.2124G>A (p.Ser708=)	rs140977837	0.00230
NM_002335.4(LRP5):c.1801+725G>A	rs576510976	0.00128
NM_002335.4(LRP5):c.34CTG[10] (p.Leu20dup)	rs72555376

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