rs2061305104
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61683568
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3478A>G (p.Asn1160Asp)
Allele
C
Clinical Significance
Uncertain significance