List of variants in gene UNC119 reported as likely benign for retinal disorder

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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
NM_005148.4(UNC119):c.*7G>A	rs370209476	0.00004
NM_005148.4(UNC119):c.*385T>C	rs541479092
NM_005148.4(UNC119):c.509A>G (p.Gln170Arg)	rs561712812
NM_005148.4(UNC119):c.586T>C (p.Phe196Leu)	rs145972313

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