List of variants in gene FAR1 reported as likely pathogenic for not provided

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_032228.6(FAR1):c.1438C>T (p.Arg480Cys)	rs12799308
NM_032228.6(FAR1):c.1439G>A (p.Arg480His)	rs1057517926
NM_032228.6(FAR1):c.955+1G>A

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