"Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabet - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 265837	NM_001035.3(RYR2):c.4069G>A (p.Asp1357Asn)	LOC126806067, RYR2 (D1357N)	Single nucleotide variant (missense variant)	Cardiomyopathy +1 more	GUncertain significance
Select item 265827	NM_001035.3(RYR2):c.8783A>G (p.Gln2928Arg)	RYR2 (Q2928R)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 4	GUncertain significance