"Genome-Nilou Lab"[submitter] AND "RIPPLY2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1165051	NM_001009994.3(RIPPLY2):c.12G>A (p.Ala4=)	RIPPLY2, RIPPLY2-CYB5R4	Single nucleotide variant (synonymous variant)	Spondylocostal dysostosis 6, autosomal recessive +1 more	GBenign
Select item 1166321	NM_001009994.3(RIPPLY2):c.96-4G>A	RIPPLY2, RIPPLY2-CYB5R4	Single nucleotide variant (non-coding transcript variant +1 more)	Spondylocostal dysostosis 6, autosomal recessive +1 more	GBenign