List of variants in gene APTX reported as likely benign by Ambry Genetics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001195248.2(APTX):c.742T>A (p.Leu248Met)	rs141195622	0.00183
NM_001195248.2(APTX):c.214G>A (p.Val72Ile)	rs367998288	0.00005
NM_001195248.2(APTX):c.35G>A (p.Ser12Asn)	rs781480218	0.00005
NM_001195248.2(APTX):c.649G>A (p.Ala217Thr)

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