rs200313246
- Uncertain significance
Your Genotype
Sign InDescription
In silico analysis, which includes protein predictors and evolutionary conservation, supports a deleterious effect
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
A
Alternative Allele
T
Chromosome
22
Location
37769084
Variant Type
SNP
Genes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6632A>T (p.Gln2211Leu)
Allele
T
Clinical Significance
Uncertain significance