rs778500245
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
C
Alternative Allele
A
T
Chromosome
17
Location
61683974
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3072G>A (p.Gly1024=)
Allele
T
Clinical Significance
Likely benign