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INS

insulin

HCNC Approved Symbol
INS (HGNC:6081)
Genomic Coordinates
11:2,159,779 - 2,161,209 (11p15.5)
Synonyms
IDDM2, IDDM1
Disease Associations
This gene is associated with the following 4 diseases in OMIM.

Diagnosed Cases

1Patient

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

Frequently observed phenotypes

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

Hyperglycemia
 1 (100.0%)
INS - Gene browser | 3billion