C3553831[trait identifier] AND "Centre for Mendelian Genomics, Univers - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 931427	NM_173630.4(RTTN):c.1067T>C (p.Met356Thr)	RTTN (M356T)	Single nucleotide variant (5 prime UTR variant +1 more)	Microcephalic primordial dwarfism due to RTTN deficiency	GUncertain significance
Select item 930363	NM_173630.4(RTTN):c.29T>C (p.Leu10Pro)	RTTN (L10P)	Single nucleotide variant (5 prime UTR variant +1 more)	Microcephalic primordial dwarfism due to RTTN deficiency	GUncertain significance