rs2061322186
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
17
Location
61683999
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3047T>G (p.Ile1016Arg)
Allele
C
Clinical Significance
Uncertain significance