rs1567728640
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
17
Location
61683805
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3241G>A (p.Ala1081Thr)
Allele
T
Clinical Significance
Uncertain significance