rs1555572922
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
17
Location
61684053
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.2993A>G (p.Lys998Arg)
Allele
C
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.2993A>T (p.Lys998Met)
Allele
A
Clinical Significance
Uncertain significance