rs1034551306
- Uncertain significance
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
G
Chromosome
17
Location
61683624
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3422A>T (p.Asp1141Val)
Allele
A
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3422A>C (p.Asp1141Ala)
Allele
G
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3422A>G (p.Asp1141Gly)
Allele
C
Clinical Significance
Uncertain significance