Gene CD36 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: CD36
Disorder: Platelet glycoprotein IV deficiency
Allele Frequency: 0.0171692
Carrier Rate: 0.0337488
Max At-Risk Couples rate: 0.00113898
The table below lists all clinically relevant variants identified in the CD36 gene based on the Emirati cohort dataset.
| id |
Chromosome Position |
Gene Name |
HGVS c. (Clinically Relevant) |
HGVS p. (Clinically Relevant) |
Allele Count |
Allele Frequency |
| 8 |
80302709 |
CD36 |
NM_001001547.3:c.1240_1243dupCTTT |
NP_001001547.1:p.Trp415Serfs*4 |
30 |
0.012563% |
| 59 |
80300333 |
CD36 |
NM_001001547.3:c.859G>T |
NP_001001547.1:p.Gly287Ter |
6 |
0.002513% |
| 290 |
80293720 |
CD36 |
NM_001001547.3:c.610-2A>G |
|
2 |
0.000838% |
| 752 |
80285911 |
CD36 |
NM_001001547.3:c.176delC |
NP_001001547.1:p.Thr59Lysfs*18 |
1 |
0.000419% |
| 753 |
80301236 |
CD36 |
NM_001001547.3:c.1007-2A>G |
|
1 |
0.000419% |
| 754 |
80302726 |
CD36 |
NM_001001547.3:c.1254+1G>C |
|
1 |
0.000419% |
