Variants with conflicting interpretations "likely pathogenic" from Amrita Institute of Medical Sciences and Research Centre, Amrita Vishwa Vidyapeetham and "pathogenic" from any submitter

Minimum review status of the submission from Amrita Institute of Medical Sciences and Research Centre, Amrita Vishwa Vidyapeetham:		Collection method of the submission from Amrita Institute of Medical Sciences and Research Centre, Amrita Vishwa Vidyapeetham:
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.1027G>A (p.Gly343Ser)
NM_000527.5(LDLR):c.530C>T (p.Ser177Leu)
NM_000527.5(LDLR):c.727T>C (p.Cys243Arg)	rs879254659

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