ClinVar Miner

List of variants in gene MORC2 reported as likely pathogenic by Undiagnosed Diseases Network, NIH

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001303256.3(MORC2):c.1265A>G (p.Glu422Gly)	rs2040680054
NM_001303256.3(MORC2):c.394C>T (p.Arg132Cys)	rs1064795559

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