Related gene-specific medical variations for Gene (Select 10873) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2533064	NM_001161586.3(ME3):c.1557A>T (p.Gln519His)	LOC126861285, ME3 (Q519H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342312	NM_001161586.3(ME3):c.1625G>A (p.Arg542Gln)	LOC126861285, ME3 (R542Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1527658	GRCh37/hg19 11q14.2(chr11:86217857-86429093)	ME3	Copy number loss	not specified	GUncertain significance
Select item 815451	GRCh37/hg19 11q14.2(chr11:86217857-86429093)x1	ME3	Copy number loss	not provided	GLikely benign

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