List of variants in gene RAB7A 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004637.6(RAB7A):c.495G>A (p.Ala165=)	rs146566121	0.00341
NM_004637.6(RAB7A):c.423C>G (p.Ala141=)	rs61758751	0.00210
NM_004637.6(RAB7A):c.87G>A (p.Val29=)	rs145441548	0.00039
NM_004637.6(RAB7A):c.213G>A (p.Gln71=)	rs140299645	0.00007
NM_004637.6(RAB7A):c.183A>C (p.Ile61=)	rs376642691	0.00002
NM_004637.6(RAB7A):c.21G>A (p.Val7=)	rs140857794	0.00001
NM_004637.6(RAB7A):c.321C>T (p.Leu107=)	rs749227632	0.00001
NM_004637.6(RAB7A):c.414G>T (p.Arg138=)	rs754928233

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