List of variants in gene LRP5 reported as benign by Eurofins NTD LLC (GA)

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_002335.4(LRP5):c.884-4T>C	rs314776	0.48379
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.4000+10T>A	rs116068042	0.02476
NM_002335.4(LRP5):c.4574C>T (p.Ala1525Val)	rs1127291	0.01003
NM_002335.4(LRP5):c.266A>G (p.Gln89Arg)	rs41494349	0.00826
NM_002335.4(LRP5):c.687-8G>A	rs190810239	0.00718
NM_002335.4(LRP5):c.16C>A (p.Pro6Thr)	rs771718186	0.00289
NM_002335.4(LRP5):c.4209C>G (p.Val1403=)	rs147671915	0.00226
NM_002335.4(LRP5):c.1968C>T (p.His656=)	rs144847027	0.00194
NM_002335.4(LRP5):c.4380C>T (p.Ser1460=)	rs11574420	0.00182
NM_002335.4(LRP5):c.2295G>A (p.Ser765=)	rs140955013	0.00156
NM_002335.4(LRP5):c.2193C>T (p.Asn731=)	rs147388442	0.00108
NM_002335.4(LRP5):c.1392C>T (p.Ile464=)	rs569443429
NM_002335.4(LRP5):c.34CTG[10] (p.Leu20dup)	rs72555376
NM_002335.4(LRP5):c.4458G>T (p.Ser1486=)	rs75571306

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