rs1555572663
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
17
Location
61683688
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3358G>A (p.Asp1120Asn)
Allele
T
Clinical Significance
Uncertain significance