rs2061308538
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
17
Location
61683644
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3402T>G (p.Pro1134=)
Allele
C
Clinical Significance
Likely benign