rs1603275371
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
17
Location
61683813
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3233A>C (p.Lys1078Thr)
Allele
G
Clinical Significance
Uncertain significance