List of variants in gene F9 reported as benign for not specified

Minimum submission review status:		Collection method:
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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000133.4(F9):c.580A>G (p.Thr194Ala)	rs6048	0.22614
NM_000133.4(F9):c.1095A>G (p.Ser365=)	rs112057482	0.01021
NM_000133.4(F9):c.1110G>A (p.Gln370=)	rs34698779	0.00833
NM_000133.4(F9):c.967G>A (p.Glu323Lys)	rs150351950	0.00294
NM_000133.4(F9):c.391+10T>G	rs375734226	0.00116
NM_000133.4(F9):c.839-20dup	rs773613916

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