List of variants in gene SLC7A7 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003982.4(SLC7A7):c.439C>T (p.Leu147Phe)	rs146280056	0.00005
NM_003982.4(SLC7A7):c.1381A>G (p.Ile461Val)	rs147383728	0.00003
NM_003982.4(SLC7A7):c.932T>C (p.Ile311Thr)

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