rs1603275620
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
17
Location
61684050
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2996G>T (p.Arg999Ile)
Allele
A
Clinical Significance
Uncertain significance