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SNP information rs11697186

RS11697186

Normal allele: AA

Polymorphism causing the risk of thrombocytopenia during pegylated interferon and ribavirin therapy for chronic hepatitis C.

Polymorphism rs11697186 is related to topics like this:

Hepatitis genetic

Genetic factors can play an important role in treatment response and disease progression in chronic...


Lupus is it genetic

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Crohn's disease genetic

A chronic disorder known as Crohn's disease is a multi-faceted condition that primarily impacts the...

Is rheumatoid arthritis genetic

Chronic abnormal inflammation is the hallmark of rheumatoid arthritis, a disease that primarily...

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