List of variants in gene FH reported as likely pathogenic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000143.4(FH):c.923C>G (p.Ala308Gly)	rs1057524385	0.00001
NM_000143.4(FH):c.1431_1433dup (p.Lys477dup)	rs367543046
NM_000143.4(FH):c.3G>A (p.Met1Ile)	rs564147469
NM_000143.4(FH):c.462T>G (p.Asn154Lys)	rs2147921891

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