List of variants in gene AP1B1 reported as uncertain significance for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001127.4(AP1B1):c.1280G>T (p.Ser427Ile)	rs1183324698
NM_001127.4(AP1B1):c.1702G>A (p.Gly568Ser)
NM_001127.4(AP1B1):c.2259C>A (p.Asn753Lys)	rs2147939173
NM_001127.4(AP1B1):c.2524_2524+3dup	rs2147931230
NM_001127.4(AP1B1):c.565G>C (p.Glu189Gln)	rs570779704
NM_001127.4(AP1B1):c.581G>A (p.Ser194Asn)
NM_001127.4(AP1B1):c.637G>A (p.Glu213Lys)	rs1569159579

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