rs199776134
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
8
Location
68077406
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.1579C>A (p.Arg527Ser)
Allele
A
Clinical Significance
Uncertain significance