rs896510433
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
17
Location
61683903
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3143C>T (p.Pro1048Leu)
Allele
A
Clinical Significance
Uncertain significance