"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "F12"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1169	NM_000505.4(F12):c.983C>A (p.Thr328Lys)	F12, SLC34A1 (T328K)	Single nucleotide variant (missense variant)	Hereditary angioneurotic edema +3 more	GPathogenic
Select item 2904978	NM_000505.4(F12):c.115G>A (p.Val39Ile)	F12 (V39I)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 369462	NC_000005.10:g.177409584C>G	F12	Single nucleotide variant	Hereditary angioneurotic edema +3 more	GConflicting classifications of pathogenicity

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