rs2061317418
- Uncertain significance
Your Genotype
Sign InDescription
Curator: Arleen D. Auerbach. Submitter to LOVD: Yukihide Momozawa.
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61683866
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.3180A>G (p.Val1060=)
Allele
C
Clinical Significance
Uncertain significance