rs1275343223
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
17
Location
61683724
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3322G>A (p.Val1108Ile)
Allele
T
Clinical Significance
Uncertain significance