rs1060504321
- Likely benign
Your Genotype
Sign InDescription
In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61685873
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2868A>G (p.Ser956=)
Allele
C
Clinical Significance
Likely benign