rs765416041
- Uncertain significance
Your Genotype
Sign InDescription
Has not been previously published as pathogenic or benign to our knowledge; Not observed at a significant frequency in large population cohorts (Lek 2016); In silico analysis supports that this missense variant does not alter protein structure/function
Reference Allele
G
Alternative Allele
T
Chromosome
17
Location
61683946
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3100C>A (p.Pro1034Thr)
Allele
T
Clinical Significance
Uncertain significance