[ensembl-dev] Rest

Igo Medeiros igo701 at gmail.com
Mon Jun 29 17:59:50 BST 2015


Thank you for help.
I have other question about rest.
I am using this link
http://grch37.rest.ensembl.org/vep/human/region/22:30163533-30163533/C? to
find a mutation, but i noticed that when i use
http://grch37.rest.ensembl.org/overlap/region/human/22:30162533-30165533?feature=variation;
i don't find, in this interval, the mutation that i found in rest.vep.
Is there some way that i can pass the interval in rest.vep whitout the
allele?

Thank you for attention.

2015-06-29 8:52 GMT-03:00 Will McLaren <wm2 at ebi.ac.uk>:

> Hello,
>
> The variation ID endpoint gives clinical significance and phenotype
> (disease) information, e.g.
>
>
> http://rest.ensembl.org/variation/human/rs699?content-type=application/json&phenotypes=1
>
> Documentation is here:
> http://rest.ensembl.org/documentation/info/variation_id
>
> Study information is not currently available via our REST API.
>
> Regards
>
> Will McLaren
> Ensembl Variation
>
> On 29 June 2015 at 12:15, Igo Medeiros <igo701 at gmail.com> wrote:
>
>> Hi ENsembl Team,
>> I am using rest, but I need the information about clinical significance,
>> disease and study, but I am not find there. How can I find this
>> informations in rest?
>> I was looking at documentation, but not found.
>>
>> --
>> Igo Paixão de Medeiros
>>
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>>
>
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>


-- 
Igo Paixão de Medeiros
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