"RBBP6-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2443234	NM_006910.5(RBBP6):c.4311A>G (p.Gln1437=)	RBBP6	Single nucleotide variant (synonymous variant)	RBBP6-related disorder	GLikely benign
Select item 3047291	NM_006910.5(RBBP6):c.4460G>A (p.Arg1487His)	RBBP6 (R1453H +1 more)	Single nucleotide variant (missense variant)	RBBP6-related disorder	GLikely benign
Select item 3042574	NM_006910.5(RBBP6):c.4490G>A (p.Arg1497Gln)	RBBP6 (R1463Q +1 more)	Single nucleotide variant (missense variant)	RBBP6-related disorder	GLikely benign

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