List of variants in gene RAB7A reported as uncertain significance 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_004637.6(RAB7A):c.167T>C (p.Leu56Pro)	rs775104487	0.00003
NM_004637.6(RAB7A):c.503C>T (p.Thr168Met)	rs141978327	0.00003
NM_004637.6(RAB7A):c.257T>C (p.Leu86Pro)

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