rs1555572792
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
G
Alternative Allele
A
Chromosome
17
Location
61683863
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3183C>T (p.Asn1061=)
Allele
A
Clinical Significance
Likely benign