rs1555572994
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
17
Location
61684138
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2908G>A (p.Asp970Asn)
Allele
T
Clinical Significance
Uncertain significance