rs116570374
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
8
Location
68192466
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.4545G>A (p.Ser1515=)
Allele
A
Clinical Significance
Benign