rs1358278249
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61683776
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3270A>G (p.Glu1090=)
Allele
C
Clinical Significance
Likely benign