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SNP information rs201381904

RS201381904

Normal allele: CC

A 10-fold higher risk of venous thromboembolism among rs201381904(T) carriers despite normal levels of antithrombin and anticoagulant activity.

Polymorphism rs201381904 is related to topics like this:

G20210A prothrombin mutation

The Prothrombin G20210A mutation, also known as Factor II mutation, is a hereditary trait that...

Schizophrenia is it genetic

A psychosis known as schizophrenia impacts an individual's thinking, sense of self, and...

Hereditary polyneuropathy

The peripheral nervous system is affected by a diverse range of diseases known as hereditary...

Melanoma genes

The incidence of malignant melanoma (MM) is rising sharply, making it one of the most aggressive...

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