rs968860042
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
17
Location
61683712
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3334G>A (p.Asp1112Asn)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3334G>T (p.Asp1112Tyr)
Allele
A
Clinical Significance
Uncertain significance