ClinVar Miner

List of variants reported as likely benign for Hereditary factor XI deficiency disease by Genome-Nilou Lab

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.1717-48A>G	rs5966	0.06916
NM_000128.4(F11):c.1481-34G>T	rs2289253
NM_000128.4(F11):c.1576+51C>A	rs2289254

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