rs2061317245
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
17
Location
61683864
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.3182A>T (p.Asn1061Ile)
Allele
A
Clinical Significance
Uncertain significance