rs1567731036
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Not observed in large population cohorts (Lek et al., 2016); In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Reference Allele
G
Alternative Allele
A
C
Chromosome
17
Location
61685865
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2876C>G (p.Pro959Arg)
Allele
C
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.2876C>T (p.Pro959Leu)
Allele
A
Clinical Significance
Uncertain significance