Variants in gene VPS13B with conflicting interpretations "likely pathogenic" and "likely benign"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.7708G>A (p.Asp2570Asn)	rs140179844	0.00117
NM_152564.5(VPS13B):c.5803T>G (p.Ser1935Ala)	rs138930771	0.00053
NM_152564.5(VPS13B):c.11750_11752dup (p.Asp3917dup)	rs386834068
NM_152564.5(VPS13B):c.9337_9338del (p.Arg3113fs)	rs754443525

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