List of variants in gene NTHL1 reported as benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002528.7(NTHL1):c.116-17C>T	rs2233518	0.01075
NM_002528.7(NTHL1):c.116-37T>C	rs3211968	0.00990
NM_002528.7(NTHL1):c.116-10C>G	rs3211970	0.00366
NM_002528.7(NTHL1):c.354+30dup	rs3211971

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