ClinVar Miner

List of variants in gene AP4B1 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001253852.3(AP4B1):c.682C>T (p.Arg228Cys)	rs371514044	0.00004
NM_001253852.3(AP4B1):c.202G>A (p.Val68Ile)	rs751780972	0.00001

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