Related gene-specific medical variations for Gene (Select 5928) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3172662	NM_030786.3(SYNC):c.1387C>G (p.Gln463Glu)	RBBP4, SYNC (Q463E)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2487930	NM_030786.3(SYNC):c.1292A>G (p.Gln431Arg)	RBBP4, SYNC (Q431R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2306637	NM_030786.3(SYNC):c.1336G>A (p.Ala446Thr)	RBBP4, SYNC (A446T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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