rs727503529
- Benign/Likely benign
Your Genotype
Sign InDescription
c.6936+13G>T in intron 22 of TRIOBP: This variant is not expected to have clinic al significance because it does not alter an amino acid residue and is not locat ed within the splice consensus sequence. It has been identified in 0.2% (69/3358 0) of Latino chromosomes, including 1 homozygote, by the Genome Aggregation Data base (gnomAD, http://gnomad.broadinstitute.org; dbSNP rs727503529).
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
22
Location
37771749
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6936+13G>T
Allele
T
Clinical Significance
Benign/Likely benign