rs748928248
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
17
Location
61683752
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3294C>T (p.Ala1098=)
Allele
A
Clinical Significance
Likely benign