List of variants in gene combination F12, SLC34A1 reported as benign for Factor XII deficiency disease

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003052.5(SLC34A1):c.*202A>C	rs6556319	0.03226
NM_003052.5(SLC34A1):c.1635C>T (p.Gly545=)	rs7379524	0.02591
NM_000505.4(F12):c.1251-9C>T	rs17876032

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