Variants in gene SPTA1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 6

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HGVS	dbSNP
NM_003126.4(SPTA1):c.2909C>A (p.Ala970Asp)	rs35948326
NM_003126.4(SPTA1):c.5572C>G (p.Leu1858Val)	rs3737515
NM_003126.4(SPTA1):c.6559A>G (p.Lys2187Glu)	rs111980420
NM_003126.4(SPTA1):c.6789-19_6789-18dup	rs5778083
NM_003126.4(SPTA1):c.6789-19dup	rs5778083
NM_003126.4(SPTA1):c.6789-8del	rs5778083

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