rs1555572908
- Conflicting interpretations of pathogenicity
- Uncertain significance
Your Genotype
Sign InDescription
In silico models in agreement (benign);Other strong data supporting benign classification
Reference Allele
C
Alternative Allele
A
T
Chromosome
17
Location
61684020
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3026G>A (p.Gly1009Glu)
Allele
T
Clinical Significance
Conflicting interpretations of pathogenicity
Name
NM_032043.3(BRIP1):c.3026G>T (p.Gly1009Val)
Allele
A
Clinical Significance
Uncertain significance