Variants in gene MOCS1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001358530.2(MOCS1):c.484C>T (p.Arg162Trp)	rs746138504	0.00006
NM_001358530.2(MOCS1):c.1150+20G>A	rs752653792	0.00001
NM_001358530.2(MOCS1):c.1150G>A (p.Glu384Lys)	rs751603831	0.00001

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