Variants with conflicting interpretations "likely benign" from Fundacion Hipercolesterolemia Familiar and "uncertain significance" from any submitter

Minimum review status of the submission from Fundacion Hipercolesterolemia Familiar:		Collection method of the submission from Fundacion Hipercolesterolemia Familiar:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.2140+5G>A	rs72658867	0.00757
NM_000527.5(LDLR):c.1706-10G>A	rs17248882	0.00154
NM_000527.5(LDLR):c.806G>A (p.Gly269Asp)	rs143992984	0.00026

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