"PreventionGenetics, part of Exact Sciences"[submitter] AND "RAB7A"[ge - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 343156	NM_004637.6(RAB7A):c.-18A>G	RAB7A	Single nucleotide variant (5 prime UTR variant)	RAB7A-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 464094	NM_004637.6(RAB7A):c.21G>A (p.Val7=)	RAB7A	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +4 more	GLikely benign
Select item 343157	NM_004637.6(RAB7A):c.87G>A (p.Val29=)	RAB7A	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +4 more	GBenign/Likely benign
Select item 285287	NM_004637.6(RAB7A):c.423C>G (p.Ala141=)	RAB7A	Single nucleotide variant (synonymous variant)	not specified +5 more	GBenign/Likely benign
Select item 343160	NM_004637.6(RAB7A):c.552C>T (p.Asn184=)	LOC112872299, RAB7A	Single nucleotide variant (synonymous variant)	RAB7A-related disorder +2 more	GLikely benign

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