Related gene-specific medical variations for Gene (Select 10325) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3156371	NM_006064.5(RRAGB):c.38A>G (p.Glu13Gly)	LOC130068334, RRAGB (E13G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2548813	NM_006064.5(RRAGB):c.40A>G (p.Asn14Asp)	LOC130068334, RRAGB (N14D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 394447	GRCh37/hg19 Xp11.21(chrX:55745691-55932670)x3	RRAGB	Copy number gain	See cases	GLikely benign

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