rs369340444
- Uncertain significance
Your Genotype
Sign InDescription
Curator: Arleen D. Auerbach. Submitter to LOVD: Yukihide Momozawa.
Reference Allele
C
Alternative Allele
G
T
Chromosome
17
Location
61683643
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3403G>C (p.Glu1135Gln)
Allele
G
Clinical Significance
Uncertain significance