Variants in gene LRP5 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_002335.4(LRP5):c.685C>T (p.Arg229Trp)	rs766589610	0.00006
NM_002335.4(LRP5):c.1321G>A (p.Glu441Lys)	rs376152274	0.00001
NM_002335.4(LRP5):c.2555C>T (p.Thr852Met)	rs1398692057	0.00001
NM_002335.4(LRP5):c.1481G>A (p.Arg494Gln)	rs121908664
NM_002335.4(LRP5):c.1828G>A (p.Gly610Arg)	rs80358313
NM_002335.4(LRP5):c.1A>G (p.Met1Val)	rs2153110162
NM_002335.4(LRP5):c.209_210delinsAA (p.Phe70Ter)	rs2098614719
NM_002335.4(LRP5):c.593A>G (p.Asn198Ser)	rs1085307078
NM_002335.4(LRP5):c.724G>A (p.Ala242Thr)	rs121908670

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