"Clinical Genetics, Academic Medical Center"[submitter] AND "LOC129993 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 538137	NM_001034850.3(RETREG1):c.18T>G (p.Pro6=)	LOC129993734, RETREG1 +1 more	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 286856	NM_001034850.3(RETREG1):c.-19T>C	LOC129993734, RETREG1 +1 more	Single nucleotide variant (5 prime UTR variant)	Neuropathy, hereditary sensory and autonomic, type 2B +1 more	GBenign