rs1555573005
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
17
Location
61684148
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2906-8A>G
Allele
C
Clinical Significance
Likely benign
T
C
17
61684148
SNP
NM_032043.3(BRIP1):c.2906-8A>G
C
Likely benign