"GeneDx"[submitter] AND "MROH8"[gene] - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59195	GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3	LOC613266, MACROD2 +950 more	Copy number gain	See cases	GPathogenic
Select item 1238363	NC_000020.11:g.37178722C>A	MROH8, RPN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249784	NC_000020.11:g.37178751A>T	MROH8, RPN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253465	NC_000020.11:g.37178834C>T	MROH8, RPN2	Single nucleotide variant (intron variant)	not provided	GBenign

Format

Sort by

Choose Destination

ClinVar