rs1567727955
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
17
Location
61683609
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3437A>G (p.Lys1146Arg)
Allele
C
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3437A>T (p.Lys1146Ile)
Allele
A
Clinical Significance
Uncertain significance