List of variants in gene RMND1 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017909.4(RMND1):c.713A>G (p.Asn238Ser)	rs144972972	0.00013
NM_017909.4(RMND1):c.1200+1G>A
NM_017909.4(RMND1):c.291del (p.Thr97_Met98insTer)	rs763658299
NM_017909.4(RMND1):c.494_497del (p.Leu164_Ser165insTer)	rs1427212110
NM_017909.4(RMND1):c.729+1_729+2del

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