rs786201171
- Likely benign
Your Genotype
Sign InDescription
In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61684019
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3027A>G (p.Gly1009=)
Allele
C
Clinical Significance
Likely benign