rs2061324725
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
17
Location
61684074
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2972C>T (p.Pro991Leu)
Allele
A
Clinical Significance
Uncertain significance