rs1315917374
- Likely benign
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
T
Chromosome
17
Location
61683617
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3429T>C (p.Asp1143=)
Allele
G
Clinical Significance
Likely benign
Name
NM_032043.3(BRIP1):c.3429T>G (p.Asp1143Glu)
Allele
C
Clinical Significance
Uncertain significance