rs1057518847
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
This variant was classified as: Uncertain significance.
Reference Allele
T
Alternative Allele
A
C
Chromosome
17
Location
61683633
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3413A>G (p.Asp1138Gly)
Allele
C
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3413A>T (p.Asp1138Val)
Allele
A
Clinical Significance
Uncertain significance