rs755337038
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
17
Location
61684099
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2947A>T (p.Ile983Phe)
Allele
A
Clinical Significance
Uncertain significance