List of variants in gene SERPINC1 reported as benign for inherited thrombophilia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.1011A>G (p.Gln337=)	rs5878	0.48194
NM_000488.4(SERPINC1):c.981A>G (p.Val327=)	rs5877	0.47782
NM_000488.4(SERPINC1):c.1154-53G>A	rs2759328	0.09980
NM_000488.4(SERPINC1):c.1218+27G>C	rs677	0.09086
NM_000488.4(SERPINC1):c.42-18C>T	rs2227599	0.02345
NM_000488.4(SERPINC1):c.439A>G (p.Thr147Ala)	rs2227606	0.00184
NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu)	rs2227624	0.00167
NM_000488.4(SERPINC1):c.678C>T (p.Thr226=)	rs2227627	0.00045
NM_000488.4(SERPINC1):c.1005G>A (p.Val335=)	rs192187532	0.00031
NM_000488.4(SERPINC1):c.763-16T>C	rs145418597	0.00026
NM_000488.4(SERPINC1):c.873T>C (p.Arg291=)	rs775845871	0.00026
NM_000488.4(SERPINC1):c.1154-5T>C	rs375346550	0.00007
NM_000488.4(SERPINC1):c.914C>A (p.Pro305His)	rs549991084	0.00001
NM_000488.4(SERPINC1):c.409-12del	rs201656611
NM_000488.4(SERPINC1):c.409-12dup	rs201656611
NM_000488.4(SERPINC1):c.693C>G (p.Thr231=)	rs140452859
NM_000488.4(SERPINC1):c.693C>T (p.Thr231=)	rs140452859

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