ClinVar Miner

List of variants in gene F13A1 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (45):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
NM_000129.3(F13A1):c.*1030G>T rs548323382
NM_000129.3(F13A1):c.*1167T>G rs886061655
NM_000129.3(F13A1):c.*270C>T rs568780978
NM_000129.3(F13A1):c.*417G>T rs886061658
NM_000129.3(F13A1):c.*42G>A rs886061659
NM_000129.3(F13A1):c.*443G>A rs3024486
NM_000129.3(F13A1):c.*587G>A rs75981686
NM_000129.3(F13A1):c.*619C>T rs191569585
NM_000129.3(F13A1):c.*627G>A rs886061657
NM_000129.3(F13A1):c.*628G>A rs886061656
NM_000129.3(F13A1):c.*67C>T rs182425546
NM_000129.3(F13A1):c.*927G>A rs746364189
NM_000129.3(F13A1):c.*945T>C rs774737661
NM_000129.3(F13A1):c.-28G>A rs886061662
NM_000129.3(F13A1):c.102C>T (p.Gly34=) rs187027323
NM_000129.3(F13A1):c.1112+11T>C rs758486753
NM_000129.3(F13A1):c.160T>A (p.Phe54Ile) rs138690353
NM_000129.3(F13A1):c.1731G>C (p.Thr577=) rs137945179
NM_000129.3(F13A1):c.1860G>C (p.Leu620=) rs138943514
NM_000129.3(F13A1):c.2029A>G (p.Met677Val) rs371964182
NM_000129.3(F13A1):c.2067C>T (p.Thr689=) rs750971578
NM_000129.3(F13A1):c.327C>T (p.Tyr109=) rs886061661
NM_000129.3(F13A1):c.782G>A (p.Arg261His) rs121913071
NM_000129.3(F13A1):c.799-13C>T rs188094485
NM_000129.3(F13A1):c.889G>A (p.Val297Ile) rs199564311
NM_000129.3(F13A1):c.990A>T (p.Gly330=) rs886061660

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