Rare Myeloproliferative Variants Registry

The aims of the RaMP-Var registry are:

  • To collect clinical, histological and laboratory data on UK patients investigated for an MPN who have uncommon variants identified on myeloid gene panel

  • To share data between UK haematopathology and genomic laboratories to facilitate prospective interpretation of similar variants as these are analysed and reported.

We are grateful to the British Society of Haematology for their support from a Genomics Grant.

Get involved

Collaborate

If you’re interested in collaborating, please fill out the form, and we will get back to you.
Alternatively email us at: cuh.ramp-var@nhs.net