rs111417126
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
68069124
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.1431C>T (p.Asp477=)
Allele
T
Clinical Significance
Benign
C
T
8
68069124
SNP
NM_024870.4(PREX2):c.1431C>T (p.Asp477=)
T
Benign