rs1424179519
- Likely benign
- Uncertain significance
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
A
Alternative Allele
C
G
Chromosome
17
Location
61683962
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3084T>C (p.Asn1028=)
Allele
G
Clinical Significance
Likely benign
Name
NM_032043.3(BRIP1):c.3084T>G (p.Asn1028Lys)
Allele
C
Clinical Significance
Uncertain significance