rs1603275650
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
17
Location
61684076
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2970C>T (p.Ser990=)
Allele
A
Clinical Significance
Likely benign