C11orf21[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2359387	NM_001329958.2(C11orf21):c.163A>G (p.Met55Val)	C11orf21 (M55V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3135659	NM_001329958.2(C11orf21):c.54-147C>T	C11orf21 (L39F)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2397903	NM_001329958.2(C11orf21):c.41C>T (p.Pro14Leu)	C11orf21 (P14L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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