rs2061304526
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
17
Location
61683549
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3497T>C (p.Leu1166Ser)
Allele
G
Clinical Significance
Uncertain significance