rs2061325330
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
17
Location
61684096
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.2950G>T (p.Val984Leu)
Allele
A
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.2950G>A (p.Val984Met)
Allele
T
Clinical Significance
Uncertain significance