List of variants in gene APTX reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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_001195248.2(APTX):c.318C>T (p.Asn106=)	rs79254654	0.00842
NM_001195248.2(APTX):c.484-25_484-3del	rs779869639
NM_001195248.2(APTX):c.484-25_484-4del	rs778542759
NM_001195248.2(APTX):c.484-25_484-5del	rs200922655
NM_001195248.2(APTX):c.484-25_484-6del	rs771925873
NM_001195248.2(APTX):c.484-3del	rs373304582

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