Variants in gene LRP5 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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.2124G>A (p.Ser708=)	rs140977837	0.00230
NM_002335.4(LRP5):c.3107G>A (p.Arg1036Gln)	rs61889560	0.00207
NM_002335.4(LRP5):c.3990G>A (p.Ala1330=)	rs147637431	0.00108
NM_002335.4(LRP5):c.2234C>T (p.Ala745Val)	rs148550774	0.00083
NM_002335.4(LRP5):c.1413-7T>A	rs141889567	0.00077
NM_002335.4(LRP5):c.4511C>T (p.Pro1504Leu)	rs201475647	0.00039
NM_002335.4(LRP5):c.3901G>A (p.Ala1301Thr)	rs149166384	0.00008
NM_002335.4(LRP5):c.-19del	rs763941232
NM_002335.4(LRP5):c.3446T>A (p.Leu1149Gln)	rs200389686

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