rs1567728614
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
17
Location
61683799
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.3247C>G (p.Leu1083Val)
Allele
C
Clinical Significance
Uncertain significance