List of variants in gene UNC119 reported as benign 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005148.4(UNC119):c.*1C>T	rs2070139	0.12907
NM_005148.4(UNC119):c.220+15G>C	rs200265148	0.00198
NM_005148.4(UNC119):c.267C>G (p.Val89=)	rs145710399	0.00084
NM_005148.4(UNC119):c.663C>T (p.Phe221=)	rs139354163	0.00038
NM_005148.4(UNC119):c.234C>T (p.Ser78=)	rs147732652	0.00018
NM_005148.4(UNC119):c.335-19del	rs3216757

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