Why this server?

Provides access to biomedical literature annotation and relationship mining based on PubTator3, allowing the retrieval of diseases and associated gene variants.

Why this server?

Provides access to NCBI's dbSNP database, allowing the retrieval of genetic variant information and SNP IDs.

Why this server?

Enables access to FHIR-based digital health solutions, which can be useful for retrieving disease information and potentially associated genetic variants.

Why this server?

Provides access to clinical trial data which could include information about diseases and associated genetic variants being studied.

Why this server?

While not directly related to genetics, it may provide demographic data relevant to disease distribution and potentially related genetic studies.