List of variants in gene UNC80 reported as pathogenic by OMIM

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001371986.1(UNC80):c.1078C>T (p.Arg360Ter)	rs200659479	0.00001
NM_001371986.1(UNC80):c.151C>T (p.Arg51Ter)	rs869025320
NM_001371986.1(UNC80):c.2033del (p.Asn678fs)	rs869025318
NM_001371986.1(UNC80):c.565G>A (p.Val189Met)	rs864321623
NM_001371986.1(UNC80):c.7805G>C (p.Arg2602Thr)	rs869025317
NM_001371986.1(UNC80):c.7955T>A (p.Leu2652Ter)	rs869025319

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