openSNP

Phenotype	Number of Users
Pulmonary Fibrosis	22
hemophilia C (factor XI deficiency is caused by "rare mutations" in the F11 gene)	16
MPN myeloproliferative neoplasms	10
abnormal brain shape	8
Biophilia	11
RCCX	7

Phenotype

Number of Users

User

Variation

Yes

Yes

Yes

Yes

Yes

Yes

Yes

Yes

Yes

Yes

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The openSNP project is licensed under the MIT License, the code is at GitHub. The data is donated into the public domain using CC0 1.0. The CSS of openSNP is provided by Bootstrap, from Twitter and is licensed under the Apache License v2.0, the search icon comes from glyphicons.