rs1419933310
- Uncertain significance
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
17
Location
61683702
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3344C>T (p.Ser1115Phe)
Allele
A
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3344C>G (p.Ser1115Cys)
Allele
C
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3344C>A (p.Ser1115Tyr)
Allele
T
Clinical Significance
Uncertain significance