rs1060504319
- Likely benign
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
T
Alternative Allele
A
C
Chromosome
17
Location
61683971
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3075A>T (p.Ser1025=)
Allele
A
Clinical Significance
Likely benign
Name
NM_032043.3(BRIP1):c.3075A>G (p.Ser1025=)
Allele
C
Clinical Significance
Likely benign