rs1555572732
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
17
Location
61683775
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3271C>T (p.His1091Tyr)
Allele
A
Clinical Significance
Uncertain significance