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RRAGD

Ras related GTP binding D

HCNC Approved Symbol
RRAGD (HGNC:19903)
Genomic Coordinates
6:89,364,616 - 89,412,273 (6q15)
Synonyms
DKFZP761H171, bA11D8.2.1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the RRAGD gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
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