Related gene-specific medical variations for Gene (Select 92241) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3313443	NM_052862.4(RCSD1):c.235A>G (p.Lys79Glu)	LOC126805908, RCSD1 (K49E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398644	NM_052862.4(RCSD1):c.221A>T (p.His74Leu)	LOC126805908, RCSD1 (H44L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance