Related gene-specific medical variations for Gene (Select 121268) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3154043	NM_144593.3(RHEBL1):c.19A>G (p.Arg7Gly)	LOC130007819, RHEBL1 (R7G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2327653	NM_144593.3(RHEBL1):c.44G>T (p.Arg15Leu)	LOC130007819, RHEBL1 (R15L)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance