Related gene-specific medical variations for Gene (Select 4199) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3124749	NM_002395.6(ME1):c.43G>C (p.Gly15Arg)	LOC129996766, ME1 (G15R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2685208	GRCh37/hg19 6q14.2(chr6:84011516-84062681)x1	ME1	Copy number loss	not provided	GUncertain significance
Select item 1808836	GRCh37/hg19 6q14.2(chr6:83970948-84088871)x1	ME1	Copy number loss	not provided	GUncertain significance
Select item 1527260	GRCh37/hg19 6q14.2(chr6:84029282-84124184)	ME1	Copy number loss	not specified	GUncertain significance
Select item 425527	GRCh37/hg19 6q14.2(chr6:84064628-84117542)x1	ME1	Copy number loss	not provided	GLikely benign
Select item 394457	GRCh37/hg19 6q14.2(chr6:84056520-84136451)x1	ME1	Copy number loss	See cases	GLikely benign

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