List of variants in gene FH reported as not provided 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000143.4(FH):c.53C>T (p.Pro18Leu)	rs201887750	0.00597
NM_000143.4(FH):c.77C>T (p.Pro26Leu)	rs187226800	0.00051
NM_000143.4(FH):c.1303G>A (p.Val435Met)	rs147528200	0.00021
NM_000143.4(FH):c.883G>A (p.Ala295Thr)	rs145843819	0.00018
NM_000143.4(FH):c.1138A>G (p.Met380Val)	rs587778362	0.00002
NM_000143.4(FH):c.1013T>C (p.Ile338Thr)	rs201975537
NM_000143.4(FH):c.37C>G (p.Pro13Ala)	rs587778360
NM_000143.4(FH):c.71C>G (p.Ser24Trp)	rs587778361

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