rs45552539
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
17
Location
61683664
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3382G>A (p.Glu1128Lys)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3382G>C (p.Glu1128Gln)
Allele
G
Clinical Significance
Uncertain significance