List of variants in gene FAM131A reported as likely benign for FAM131A-related disorder

Minimum submission review status:		Collection method:
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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_144635.5(FAM131A):c.302C>T (p.Ala101Val)	rs187325668	0.00111
NM_144635.5(FAM131A):c.999A>C (p.Pro333=)	rs771155670	0.00002
NM_144635.5(FAM131A):c.1086G>A (p.Glu362=)	rs2474214854

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