Variants in gene MCOLN1 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020533.3(MCOLN1):c.362C>T (p.Thr121Met)	rs750170007	0.00002
NM_020533.3(MCOLN1):c.681-19A>C	rs768736321	0.00001
NM_020533.3(MCOLN1):c.1336G>A (p.Val446Met)	rs754097561
NM_020533.3(MCOLN1):c.1336G>T (p.Val446Leu)	rs754097561

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