Related gene-specific medical variations for Gene (Select 10567) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312213	NM_006423.3(RABAC1):c.16G>A (p.Asp6Asn)	LOC130064541, RABAC1 (D6N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312212	NM_006423.3(RABAC1):c.44G>A (p.Gly15Glu)	LOC130064541, RABAC1 (G15E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance