rs1006002613
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61684002
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3044A>G (p.Lys1015Arg)
Allele
C
Clinical Significance
Uncertain significance