rs776129117
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61683774
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3272A>G (p.His1091Arg)
Allele
C
Clinical Significance
Uncertain significance