List of variants in gene SERPINE1 reported as likely benign for coagulation protein 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000602.5(SERPINE1):c.43G>A (p.Ala15Thr)	rs6092	0.07905
NM_000602.5(SERPINE1):c.*180C>T	rs41334349	0.00755
NM_000602.5(SERPINE1):c.*950C>T	rs536144892	0.00262
NM_000602.5(SERPINE1):c.*661T>C	rs138333231	0.00259
NM_000602.5(SERPINE1):c.*1787T>C	rs182671641	0.00218
NM_000602.5(SERPINE1):c.*1521T>A	rs180692432	0.00204
NM_000602.5(SERPINE1):c.*440T>C	rs58167134	0.00104
NM_000602.5(SERPINE1):c.357G>A (p.Ala119=)	rs6091	0.00050
NM_000602.5(SERPINE1):c.1088-9C>T	rs762527672	0.00003

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