ClinVar Miner

List of variants in gene AP1S2 reported as likely benign by Genetic Services Laboratory, University of Chicago

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001272071.2(AP1S2):c.288T>C (p.Ser96=)	rs61741688	0.01485
NM_001272071.2(AP1S2):c.289-8C>T	rs770199415	0.00016

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