List of variants in gene UNC80 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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.1806G>C (p.Gln602His)	rs200473652	0.00163
NM_001371986.1(UNC80):c.1818G>A (p.Pro606=)	rs61742726	0.00128
NM_001371986.1(UNC80):c.9471C>T (p.Thr3157=)	rs745339116	0.00029
NM_001371986.1(UNC80):c.2874C>G (p.Ala958=)	rs756648889	0.00010
NM_001371986.1(UNC80):c.7392T>A (p.Ile2464=)	rs943814896	0.00002
NM_001371986.1(UNC80):c.9297C>T (p.Ala3099=)	rs879405779	0.00001

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