rs1603275641
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61684059
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2987A>G (p.Gln996Arg)
Allele
C
Clinical Significance
Uncertain significance