rs2061308845
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
17
Location
61683656
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3390C>G (p.Ile1130Met)
Allele
C
Clinical Significance
Uncertain significance