rs2061311057
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
17
Location
61683714
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3332A>T (p.Glu1111Val)
Allele
A
Clinical Significance
Uncertain significance