rs2061318138
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
17
Location
61683889
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.3157T>C (p.Cys1053Arg)
Allele
G
Clinical Significance
Uncertain significance