rs1165704345
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
17
Location
61684024
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3022T>A (p.Leu1008Met)
Allele
T
Clinical Significance
Uncertain significance