rs1555572892
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61684001
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.3045A>G (p.Lys1015=)
Allele
C
Clinical Significance
Likely benign