rs1235908208
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61683642
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3404A>G (p.Glu1135Gly)
Allele
C
Clinical Significance
Uncertain significance