Related gene-specific medical variations for Gene (Select 100313772) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151722	GRCh38/hg38 Xq21.33(chrX:95022651-95133723)x3	MIR548M	Copy number gain	See cases	GBenign
Select item 145137	GRCh38/hg38 Xq21.33(chrX:95060190-95120944)x2	MIR548M	Copy number gain	See cases	GBenign
Select item 145135	GRCh38/hg38 Xq21.33(chrX:95060190-95120944)x3	MIR548M	Copy number gain	See cases	GBenign

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