List of variants in gene combination LOC130008712, UNG reported as uncertain significance for immune system 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_080911.3(UNG):c.124G>C (p.Asp42His)	rs377203641	0.00026
NM_080911.3(UNG):c.100G>A (p.Ala34Thr)	rs886048906
NM_080911.3(UNG):c.110C>A (p.Pro37His)	rs1205349419

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