rs2061313248
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
17
Location
61683763
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3283T>C (p.Ser1095Pro)
Allele
G
Clinical Significance
Uncertain significance