Gene HEXA Details
It offers a comprehensive overview of all clinically relevant variants linked to a specified gene. It provides detailed metrics for each variant, including chromosomal position, HGVS c. and p. notation, allele frequencies, carrier rates, and estimated metrics for at-risk couples. By combining gene-level statistics with specific variant-level data, this page enables an in-depth analysis of how particular genes contribute to disease, thus supporting both clinical interpretation and research efforts.
Gene: HEXA
Disorder: [Hex A pseudodeficiency]
Allele Frequency: 0.000837521
Carrier Rate: 0.00167364
Max At-Risk Couples rate: 0.0000028
The table below lists all clinically relevant variants identified in the HEXA gene based on the Emirati cohort dataset.
| id |
Chromosome Position |
Gene Name |
HGVS c. (Clinically Relevant) |
HGVS p. (Clinically Relevant) |
Allele Count |
Allele Frequency |
| 475 |
72637817 |
HEXA |
NM_000520.6:c.1496G>A |
NP_000511.2:p.Arg499His |
1 |
0.000419% |
| 476 |
72668312 |
HEXA |
NM_000520.6:c.2T>C |
p.Met1Thr |
1 |
0.000419% |
