Related gene-specific medical variations for Gene (Select 26070) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035971	NM_001127392.3(MYRF):c.46+2627G>C	MYRF, MYRF-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	MYRF-related disorder	GLikely benign
Select item 2663893	NM_006133.3(DAGLA):c.2437_2446del (p.Leu813fs)	DAGLA, MYRF-AS1 (L813fs)	Deletion (frameshift variant)	Autosomal dominant cerebellar ataxia	GLikely pathogenic
Select item 1246473	NM_001127392.3(MYRF):c.46+2697G>T	MYRF, MYRF-AS1	Single nucleotide variant (intron variant)	not provided	GBenign

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