rs2061308258
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
17
Location
61683639
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3407T>G (p.Leu1136Arg)
Allele
C
Clinical Significance
Uncertain significance