List of variants in gene combination BAG2, RAB23 reported as uncertain significance for Carpenter syndrome

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016277.5(RAB23):c.*1251G>A	rs182662	0.01763
NM_016277.5(RAB23):c.*920C>G	rs530900959	0.00013
NM_016277.5(RAB23):c.1665_1667dup	rs886061651	0.00005
NM_016277.5(RAB23):c.*1180ATCA[3]	rs139778770

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