List of variants in gene RNASEH1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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_002936.6(RNASEH1):c.641C>T (p.Thr214Met)	rs187577328	0.00008
NM_002936.6(RNASEH1):c.425_427dup (p.Val142_Tyr143insPhe)
NM_002936.6(RNASEH1):c.496C>T (p.Pro166Ser)

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