rs2061325944
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
17
Location
61684108
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2938G>C (p.Ala980Pro)
Allele
G
Clinical Significance
Uncertain significance