rs878855152
- Likely benign
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
C
Alternative Allele
A
T
Chromosome
17
Location
61683857
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3189G>A (p.Ser1063=)
Allele
T
Clinical Significance
Likely benign
Name
NM_032043.3(BRIP1):c.3189G>T (p.Ser1063=)
Allele
A
Clinical Significance
Likely benign