rs1603275660
- Likely benign
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
17
Location
61684087
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2959A>C (p.Arg987=)
Allele
G
Clinical Significance
Likely benign
Name
NM_032043.3(BRIP1):c.2959A>G (p.Arg987Gly)
Allele
C
Clinical Significance
Uncertain significance