ClinVar Miner

List of variants in gene SERPINE1 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_000602.4(SERPINE1):c.*1006T>C rs201434513
NM_000602.4(SERPINE1):c.*1147G>C rs886061838
NM_000602.4(SERPINE1):c.*1155T>C rs886061839
NM_000602.4(SERPINE1):c.*1192G>C rs886061840
NM_000602.4(SERPINE1):c.*1266G>C rs778538888
NM_000602.4(SERPINE1):c.*1295C>T rs372017980
NM_000602.4(SERPINE1):c.*1388G>A rs71557295
NM_000602.4(SERPINE1):c.*1443C>A rs886061841
NM_000602.4(SERPINE1):c.*1590A>G rs886061842
NM_000602.4(SERPINE1):c.*1668G>C rs886061843
NM_000602.4(SERPINE1):c.*1784del rs886061844
NM_000602.4(SERPINE1):c.*207C>T rs747135553
NM_000602.4(SERPINE1):c.*508C>A rs886061836
NM_000602.4(SERPINE1):c.*859C>T rs886061837
NM_000602.4(SERPINE1):c.*891C>T rs550508703
NM_000602.4(SERPINE1):c.*950C>T rs536144892
NM_000602.4(SERPINE1):c.-101G>A rs886061835
NM_000602.4(SERPINE1):c.-54C>T rs760811030
NM_000602.4(SERPINE1):c.-93C>T rs556803416
NM_000602.4(SERPINE1):c.1020C>T (p.Val340=) rs201351580
NM_000602.4(SERPINE1):c.191C>T (p.Ser64Leu) rs758271488
NM_000602.4(SERPINE1):c.456G>C (p.Val152=) rs200318916
NM_000602.4(SERPINE1):c.537C>T (p.Ala179=) rs376407844
NM_000602.4(SERPINE1):c.649G>A (p.Gly217Ser) rs766181190
NM_000602.4(SERPINE1):c.845T>G (p.Ile282Ser) rs750289183

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