rs375911315
- Likely benign
- Likely benign
Your Genotype
Sign InDescription
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.
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
17
Location
61683770
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3276G>A (p.Pro1092=)
Allele
T
Clinical Significance
Likely benign
Name
NM_032043.3(BRIP1):c.3276G>C (p.Pro1092=)
Allele
G
Clinical Significance
Likely benign