rs1060504333
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
17
Location
61683907
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3139T>C (p.Leu1047=)
Allele
G
Clinical Significance
Likely benign