Variants in gene VPS13D 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_015378.4(VPS13D):c.941+3A>G	rs372431023	0.00002
NM_015378.4(VPS13D):c.10562A>G (p.Asn3521Ser)	rs1557737087
NM_015378.4(VPS13D):c.10818_10821del (p.Gly3607fs)	rs1288603602
NM_015378.4(VPS13D):c.3569G>A (p.Gly1190Asp)	rs1557680919

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