rs1196759903
- 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
61683548
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3498A>G (p.Leu1166=)
Allele
C
Clinical Significance
Likely benign