rs778341139
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
17
Location
61685820
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.2905+16C>G
Allele
C
Clinical Significance
Likely benign