SNTA1 - Gene browser | 3billion

SNTA1

SNTA1

syntrophin alpha 1

HCNC Approved Symbol: SNTA1 (HGNC:11167)
Genomic Coordinates: 20:33,407,957 - 33,443,763 (20q11.21)
Synonyms: TACIP1, LQT12, SNT1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the SNTA1 gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Long qt syndrome: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Migraine: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Arrhythmias: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)

Last updated: 2024-06-30

SNTA1 - Gene browser | 3billion