List of variants in gene FAM111A reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001312909.2(FAM111A):c.782_791dup (p.Phe264fs)	rs533676902	0.00478
NM_001312909.2(FAM111A):c.1588A>G (p.Ile530Val)	rs117988338	0.00052

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