List of variants in gene SERPING1 reported as likely benign for cardiovascular disorder

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000062.3(SERPING1):c.5C>T (p.Ala2Val)	rs185342631	0.00094
NM_000062.3(SERPING1):c.686-179A>G	rs189335964	0.00091
NM_000062.3(SERPING1):c.465C>T (p.His155=)	rs201627388	0.00049
NM_000062.3(SERPING1):c.550+9C>G	rs201294420	0.00046
NM_000062.3(SERPING1):c.686-5C>G	rs28362952	0.00022
NM_000062.3(SERPING1):c.1164G>A (p.Met388Ile)	rs141529833	0.00016
NM_000062.3(SERPING1):c.244A>T (p.Thr82Ser)	rs147409450	0.00006
NM_000062.3(SERPING1):c.169G>A (p.Glu57Lys)	rs752993036	0.00004
NM_000062.3(SERPING1):c.1434C>T (p.Leu478=)	rs768058061	0.00002
NM_000062.3(SERPING1):c.686-1335T>A	rs1156278971	0.00001
NM_000062.2(SERPING1):c.-99dup	rs28362939
NM_000062.3(SERPING1):c.686-1333A>T	rs1945388566
NM_000062.3(SERPING1):c.686-1488_686-1487insT	rs1945386835

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