rs1305928655
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
17
Location
61685842
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2899G>A (p.Glu967Lys)
Allele
T
Clinical Significance
Uncertain significance