List of variants in gene F9 reported as likely benign for Hereditary factor IX 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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000133.4(F9):c.1095A>G (p.Ser365=)	rs112057482	0.01021
NM_000133.4(F9):c.967G>A (p.Glu323Lys)	rs150351950	0.00294
NM_000133.4(F9):c.*1048G>A	rs752396182	0.00125
NM_000133.4(F9):c.696T>C (p.Asp232=)	rs140835723	0.00113
NM_000133.4(F9):c.819T>C (p.Val273=)	rs1800455	0.00110
NM_000133.4(F9):c.19A>T (p.Ile7Phe)	rs150190385	0.00086
NM_000133.4(F9):c.907C>T (p.His303Tyr)	rs1801202	0.00044
NM_000133.4(F9):c.8G>A (p.Arg3His)	rs148060786	0.00042
NM_000133.4(F9):c.1029C>T (p.Asn343=)	rs145026483	0.00017
NM_000133.4(F9):c.250A>G (p.Thr84Ala)	rs201120367	0.00013
NM_000133.4(F9):c.768C>T (p.Ile256=)	rs758909063	0.00012
NM_000133.4(F9):c.1143A>G (p.Thr381=)	rs761784613	0.00011
NM_000133.4(F9):c.114C>T (p.Asn38=)	rs745353370	0.00011
NM_000133.4(F9):c.769G>A (p.Val257Ile)	rs200608775	0.00010
NM_000133.4(F9):c.523C>T (p.Pro175Ser)	rs762986355	0.00005
NM_000133.4(F9):c.*10G>C	rs186616567	0.00004
NM_000133.4(F9):c.108C>T (p.Asn36=)	rs184837275	0.00004
NM_000133.4(F9):c.582T>G (p.Thr194=)	rs754155651	0.00004
NM_000133.4(F9):c.658T>A (p.Ser220Thr)	rs777361659	0.00004
NM_000133.4(F9):c.730T>C (p.Leu244=)	rs765470577	0.00004
NM_000133.4(F9):c.834C>T (p.Val278=)	rs199844858	0.00004
NM_000133.4(F9):c.333C>T (p.Asp111=)	rs139289585	0.00003
NM_000133.4(F9):c.391+4A>G	rs749754992	0.00003
NM_000133.4(F9):c.966C>T (p.Asp322=)	rs373107855	0.00003
NM_000133.4(F9):c.130C>T (p.Pro44Ser)	rs776894974	0.00002
NM_000133.4(F9):c.48C>A (p.Thr16=)	rs768833956	0.00002
NM_000133.4(F9):c.1026G>A (p.Thr342=)	rs954954812	0.00001
NM_000133.4(F9):c.60A>G (p.Leu20=)	rs762082146	0.00001
NM_000133.4(F9):c.9C>T (p.Arg3=)	rs1335753805	0.00001
NM_000133.4(F9):c.507C>G (p.Ser169=)	rs565055999
NM_000133.4(F9):c.7C>T (p.Arg3Cys)	rs766259893

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