rs2061352600
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
17
Location
61685872
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2869C>G (p.Pro957Ala)
Allele
C
Clinical Significance
Uncertain significance