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SERPIND1

serpin family D member 1

HCNC Approved Symbol
SERPIND1 (HGNC:4838)
Genomic Coordinates
22:20,774,113 - 20,787,720 (22q11.21)
Synonyms
HC-II, HLS2, HC2, D22S673, HCF2
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the SERPIND1 gene.

Frequently observed phenotypes

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

Thromboembolism
 1 (100.0%)
SERPIND1 - Gene browser | 3billion