Related gene-specific medical variations for Gene (Select 8837) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2619452	NM_003879.7(CFLAR):c.572A>C (p.Gln191Pro)	CFLAR, CFLAR-AS1 (Q95P +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	Inborn genetic diseases	GLikely benign
Select item 2309532	NM_003879.7(CFLAR):c.659A>T (p.Gln220Leu)	CFLAR, CFLAR-AS1 (Q220L +1 more)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2214824	NM_003879.7(CFLAR):c.570C>G (p.Ile190Met)	CFLAR-AS1, CFLAR (I190M +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 783347	NM_003879.7(CFLAR):c.607C>A (p.Leu203Ile)	CFLAR, CFLAR-AS1 (L107I +1 more)	Single nucleotide variant (missense variant +3 more)	not provided	GBenign

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