List of variants in gene MECOM reported as likely pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 3q26.2(chr3:168665376-168815209)x1
NM_004991.4(MECOM):c.2803A>G (p.Asn935Asp)
NM_004991.4(MECOM):c.2906G>T (p.Arg969Leu)	rs2148891008
NM_004991.4(MECOM):c.613+1G>C

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