List of variants in gene FH reported as benign for not specified

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: 16

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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.268-22A>T	rs2275162	0.02420
NM_000143.4(FH):c.904+47G>A	rs145209119	0.01502
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.1237-18T>A	rs202206776	0.00128
NM_000143.4(FH):c.-11C>T	rs200942733	0.00113
NM_000143.4(FH):c.105G>A (p.Ser35=)	rs181655698	0.00066
NM_000143.4(FH):c.77C>T (p.Pro26Leu)	rs187226800	0.00051
NM_000143.4(FH):c.739-10T>C	rs201971572	0.00013
NM_000143.4(FH):c.1237-50TC[20]	rs144131869
NM_000143.4(FH):c.1237-50TC[23]	rs144131869
NM_000143.4(FH):c.1237-50TC[26]	rs144131869
NM_000143.4(FH):c.555+22dup	rs569920379

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