rs61729063
- Benign
Your Genotype
Sign InDescription
His2191Tyr in Exon 19 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 1.7% (57/3300) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://evs.gs.washington.edu/EVS; dbSNP rs61729063).
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
37768172
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6571C>T (p.His2191Tyr)
Allele
T
Clinical Significance
Benign