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

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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: 7

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.13710693del	rs2134191508
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.1439G>T (p.Arg480Leu)	rs1057517926
NM_032228.6(FAR1):c.163C>T (p.Arg55Ter)	rs1848291332
NM_032228.6(FAR1):c.397C>T (p.Arg133Ter)
NM_032228.6(FAR1):c.945G>A (p.Trp315Ter)	rs2134193085

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