rs1567728933
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
17
Location
61683898
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3148A>C (p.Thr1050Pro)
Allele
G
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3148A>G (p.Thr1050Ala)
Allele
C
Clinical Significance
Uncertain significance