List of variants in gene combination ANKH, OTULIN reported as benign by GeneDx

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_054027.6(ANKH):c.1366-240T>C	rs25989	0.99313
NM_054027.6(ANKH):c.1365+274T>A	rs25987	0.94437
NM_054027.6(ANKH):c.*31A>G	rs3045	0.09134
NM_054027.6(ANKH):c.1366-79G>A	rs73048824

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