rs1555572722
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
G
Alternative Allele
C
Chromosome
17
Location
61683767
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3279C>G (p.Leu1093=)
Allele
C
Clinical Significance
Likely benign