rs2061351932
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
17
Location
61685847
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2894G>A (p.Arg965Lys)
Allele
T
Clinical Significance
Uncertain significance