rs1555573260
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
G
Alternative Allele
A
Chromosome
17
Location
61685869
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2872C>T (p.Leu958=)
Allele
A
Clinical Significance
Likely benign