Related gene-specific medical variations for Gene (Select 100126338) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049137	NM_182706.5(SCRIB):c.643-4G>A	MIR937, SCRIB	Single nucleotide variant (non-coding transcript variant +1 more)	SCRIB-related condition	GLikely benign
Select item 796938	NM_182706.5(SCRIB):c.643-10C>T	MIR937, SCRIB	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign