List of variants in gene AP1S3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001039569.2(AP1S3):c.95C>T (p.Thr32Ile)	rs78536455	0.00422
NM_001039569.2(AP1S3):c.64A>G (p.Thr22Ala)	rs149183052	0.00120
NC_000002.12:g.223752827G>A
NC_000002.12:g.223752845T>C
NC_000002.12:g.223752894T>C
NM_001039569.2(AP1S3):c.292-4861C>T

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