rs747624574
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
A
Alternative Allele
G
Chromosome
17
Location
61683578
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032043.3(BRIP1):c.3468T>C (p.Asn1156=)
Allele
G
Clinical Significance
Likely benign