rs1603275193
- Likely benign
Your Genotype
Sign InDescription
Other strong data supporting benign classification
Reference Allele
T
Alternative Allele
A
Chromosome
17
Location
61683705
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.3341A>T (p.Gln1114Leu)
Allele
A
Clinical Significance
Likely benign