List of variants in gene FAM89B reported as likely benign for not specified

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_001098785.2(FAM89B):c.408C>T (p.Ser136=)	rs374813667	0.00002
NM_001098785.2(FAM89B):c.444G>A (p.Ala148=)	rs1047423258	0.00002
NM_001098785.2(FAM89B):c.370C>T (p.Leu124=)

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