rs1361161166
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
17
Location
61683753
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3293C>A (p.Ala1098Asp)
Allele
T
Clinical Significance
Uncertain significance