We have just released a new data build. Here are some highlights of this release:
New addition: EXAC
EXAC is a popular source to get population genetics summary (e.g. allele frequencies) of many observed human variants. You can now access these data from MyVariant.info programmatically (field: exac):
New addition: GRASP
New addition: SnpEff
We have now included pre-computed SnpEff annotations to almost every variants we have. You can access them under snpeff field:
GET http://myvariant.info/v1/variant/chr18:g.76754521G%3ET?fields=snpeff GET http://myvariant.info/v1/query?q=snpeff.ann.gene_name:BTK
As always, the updated information for all data sources is available from [our documentation](http://docs.myvariant.info/en/latest/doc/data.html). You can also check out [this table](http://docs.myvariant.info/en/latest/doc/data.html#available-fields) for all annotation fields (>480 fields) available from [MyVariant.info](http://myvariant.info).