rs770944170
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
17
Location
61685827
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2905+9A>C
Allele
G
Clinical Significance
Likely benign
T
G
17
61685827
SNP
NM_032043.3(BRIP1):c.2905+9A>C
G
Likely benign