rs2061321875
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61683993
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3053A>G (p.Lys1018Arg)
Allele
C
Clinical Significance
Uncertain significance