rs371118329
- Likely benign
Your Genotype
Sign InDescription
Ser2264Ser in Exon 21 of TRIOBP: This variant is not expected to have clinical s ignificance because it does not alter an amino acid residue, is not located with in the splice consensus sequence, and has been identified in 1/3292 African Amer ican chromosomes from a broad population by the NHLBI Exome Sequencing Project ( http://evs.gs.washington.edu/EVS).
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37769318
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6792G>A (p.Ser2264=)
Allele
A
Clinical Significance
Likely benign