List of variants reported as benign for Factor XII deficiency disease by Illumina Laboratory Services, Illumina

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000505.4(F12):c.619G>C (p.Ala207Pro)	rs17876030	0.96534
NM_000505.4(F12):c.-4T>C	rs1801020	0.67118
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.711C>T (p.Pro237=)	rs17876047	0.02352
NM_000505.4(F12):c.756C>T (p.Ala252=)	rs41309752	0.01977
NM_000505.4(F12):c.930G>C (p.Arg310Ser)	rs77098327	0.00359
NM_000505.4(F12):c.1251-9C>T	rs17876032

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