rs111476269
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
8
Location
68030666
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.705+8C>T
Allele
T
Clinical Significance
Benign
C
G
T
8
68030666
SNP
NM_024870.4(PREX2):c.705+8C>T
T
Benign