rs1603276512
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
17
Location
61685843
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2898G>A (p.Lys966=)
Allele
T
Clinical Significance
Likely benign