rs2061324557
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
17
Location
61684071
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2975C>A (p.Thr992Asn)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.2975C>T (p.Thr992Ile)
Allele
A
Clinical Significance
Uncertain significance