rs727503531
- Likely benign
Your Genotype
Sign InDescription
*2+10G>A in intron 23 of TRIOBP: This variant is not expected to have clinical s ignificance because it is not located within the splice consensus sequence and i s not predicted to impact splicing.
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37772774
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.*2+10G>A
Allele
A
Clinical Significance
Likely benign