HP - Gene browser

HP

haptoglobin

HCNC Approved Symbol: HP (HGNC:5141)
Genomic Coordinates: 16:72,054,505 - 72,061,055 (16q22.2)
Synonyms
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

0Patient

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

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

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