rs7813577
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
8
Location
68055823
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.1094-7T>C
Allele
C
Clinical Significance
Benign
T
C
8
68055823
SNP
NM_024870.4(PREX2):c.1094-7T>C
C
Benign