Variants with conflicting interpretations "benign" from LDLR-LOVD, British Heart Foundation and "uncertain significance" from any submitter

Minimum review status of the submission from LDLR-LOVD, British Heart Foundation:		Collection method of the submission from LDLR-LOVD, British Heart Foundation:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.90C>T (p.Asn30=)	rs72658855	0.00965
NM_000527.5(LDLR):c.1920C>T (p.Asn640=)	rs5926	0.00319
NM_000527.5(LDLR):c.507C>T (p.Asn169=)	rs146354103	0.00029
NM_000527.5(LDLR):c.48C>A (p.Leu16=)	rs565675103	0.00001
NM_000527.5(LDLR):c.1061-8T>C
NM_000527.5(LDLR):c.148G>T (p.Ala50Ser)	rs137853960
NM_000527.5(LDLR):c.690C>T (p.Asn230=)	rs879254643

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