rs777660106
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
C
Alternative Allele
G
T
Chromosome
17
Location
61683965
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3081G>A (p.Glu1027=)
Allele
T
Clinical Significance
Likely benign