Variants in gene SALL1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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_002968.3(SALL1):c.2050C>T (p.Gln684Ter)	rs1597229404
NM_002968.3(SALL1):c.601C>T (p.Gln201Ter)	rs2143450145
NM_002968.3(SALL1):c.826C>T (p.Arg276Ter)	rs104894537

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