rs876660747
- Likely benign
Your Genotype
Sign InDescription
In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
A
Alternative Allele
G
Chromosome
17
Location
61683686
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.3360T>C (p.Asp1120=)
Allele
G
Clinical Significance
Likely benign