Variants in gene VPS33B with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_018668.5(VPS33B):c.151C>A (p.Arg51=)	rs11542638	0.09422
NM_018668.5(VPS33B):c.1405+36G>A	rs116787959	0.03351
NM_018668.5(VPS33B):c.-8C>T	rs11542639	0.01125
NM_018668.5(VPS33B):c.1332G>A (p.Thr444=)	rs147407982	0.00416
NM_018668.5(VPS33B):c.363T>C (p.Tyr121=)	rs149733667	0.00337
NM_018668.5(VPS33B):c.842C>G (p.Ala281Gly)	rs115308854	0.00262
NM_018668.5(VPS33B):c.1701C>T (p.Leu567=)	rs146999653	0.00165
NM_018668.5(VPS33B):c.1166G>A (p.Arg389Gln)	rs145070485	0.00158
NM_018668.5(VPS33B):c.852+13G>A	rs188518961	0.00130
NM_018668.5(VPS33B):c.357G>A (p.Lys119=)	rs146758743	0.00120
NM_018668.5(VPS33B):c.1148T>C (p.Ile383Thr)	rs149121639	0.00114
NM_018668.5(VPS33B):c.1170+5G>A	rs201431055	0.00004

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