ClinVar Miner

List of variants in gene MCFD2 reported as likely benign for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_139279.5(MCFD2):c.*1010G>T rs138758588
NM_139279.5(MCFD2):c.*1042C>T rs111603188
NM_139279.5(MCFD2):c.*133A>T rs75416242
NM_139279.5(MCFD2):c.*1346G>T rs111535939
NM_139279.5(MCFD2):c.*1525C>G rs7596198
NM_139279.5(MCFD2):c.*1677T>G rs28770495
NM_139279.5(MCFD2):c.*1908G>C rs6743994
NM_139279.5(MCFD2):c.*1924T>C rs6715391
NM_139279.5(MCFD2):c.*2075C>T rs6743966
NM_139279.5(MCFD2):c.*2163A>G rs140937815
NM_139279.5(MCFD2):c.*2454C>A rs1051317
NM_139279.5(MCFD2):c.*2658C>T rs17035887
NM_139279.5(MCFD2):c.*2675C>G rs17035884
NM_139279.5(MCFD2):c.*3318T>C rs8861
NM_139279.5(MCFD2):c.*498A>G rs144674773
NM_139279.5(MCFD2):c.*693G>C rs28516550

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