rs61753703
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
8
Location
68146301
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.4180C>T (p.Arg1394Trp)
Allele
T
Clinical Significance
Benign