List of variants in gene FH reported as benign for hereditary peripheral neuropathy

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000143.4(FH):c.1302C>T (p.Cys434=)	rs2070080	0.03163
NM_000143.4(FH):c.309C>T (p.Ala103=)	rs10926501	0.02876
NM_000143.4(FH):c.927G>A (p.Pro309=)	rs61737760	0.02428
NM_000143.4(FH):c.53C>T (p.Pro18Leu)	rs201887750	0.00597
NM_000143.4(FH):c.1236+14C>T	rs149241949	0.00157
NM_000143.4(FH):c.77C>T (p.Pro26Leu)	rs187226800	0.00051
NM_000143.4(FH):c.702T>G (p.Thr234=)	rs201083387	0.00002
NM_000143.4(FH):c.1237-50TC[20]	rs144131869

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