List of variants in gene UNG reported as benign for hematologic disorder

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_080911.3(UNG):c.759C>G (p.Leu253=)	rs76391872	0.02053
NM_080911.3(UNG):c.*1013T>A	rs3219275	0.01781
NM_080911.3(UNG):c.291C>T (p.Ser97=)	rs3219210	0.00624
NM_080911.3(UNG):c.246G>C (p.Leu82=)	rs144083363	0.00140
NM_080911.3(UNG):c.622+10C>T	rs201555956	0.00026
NM_080911.3(UNG):c.528G>A (p.Pro176=)	rs373915335	0.00014
NM_080911.3(UNG):c.339+17A>C	rs778193117	0.00001
NM_080911.3(UNG):c.579T>G (p.Phe193Leu)
NM_080911.3(UNG):c.801+24_801+27del	rs144108564
NM_080911.3(UNG):c.801+27dup	rs144108564

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