rs1060501727
- Uncertain significance
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
T
Chromosome
17
Location
61684129
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2917T>A (p.Phe973Ile)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.2917T>C (p.Phe973Leu)
Allele
G
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.2917T>G (p.Phe973Val)
Allele
C
Clinical Significance
Uncertain significance