rs2061307264
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
17
Location
61683618
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3428A>G (p.Asp1143Gly)
Allele
C
Clinical Significance
Uncertain significance