List of variants in gene F11 reported as likely benign for Plasma factor XI deficiency

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.-54G>A	rs4253814	0.01170
NM_000128.4(F11):c.731A>G (p.Gln244Arg)	rs5969	0.00564
NM_000128.4(F11):c.663C>T (p.Pro221=)	rs142846329	0.00120
NM_000128.4(F11):c.861C>T (p.Ile287=)	rs5964	0.00107
NM_000128.4(F11):c.1020C>T (p.Asn340=)	rs149052026	0.00100
NM_000128.4(F11):c.797G>A (p.Ser266Asn)	rs145168351	0.00081
NM_000128.4(F11):c.1305-5C>T	rs375998777	0.00032
NM_000128.4(F11):c.866-9G>A	rs200218867	0.00025
NM_000128.4(F11):c.126C>T (p.Ser42=)	rs754973084	0.00024
NM_000128.4(F11):c.1255T>A (p.Ser419Thr)	rs568173895	0.00017
NM_000128.4(F11):c.1843G>A (p.Val615Met)	rs202061241	0.00016
NM_000128.4(F11):c.-57G>A	rs1043431996	0.00006
NM_000128.4(F11):c.1287C>T (p.Ala429=)	rs138122638	0.00006
NM_000128.4(F11):c.111G>A (p.Thr37=)	rs762996950	0.00004
NM_000128.4(F11):c.96A>C (p.Gly32=)	rs368183250	0.00004
NM_000128.4(F11):c.537G>A (p.Thr179=)	rs752308147	0.00003
NM_000128.4(F11):c.1518T>C (p.Asp506=)	rs367580331

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