rs61753700
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
68108323
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.2930C>T (p.Ser977Leu)
Allele
T
Clinical Significance
Likely benign