Related gene-specific medical variations for Gene (Select 79789) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3267803	NM_024734.4(CLMN):c.22T>C (p.Trp8Arg)	CLMN, LOC130056366 (W8R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060268	NM_024734.4(CLMN):c.15G>A (p.Glu5=)	CLMN, LOC130056366	Single nucleotide variant (synonymous variant)	CLMN-related disorder	GBenign
Select item 2371342	NM_024734.4(CLMN):c.46G>A (p.Gly16Arg)	CLMN, LOC130056366 (G16R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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