rs142444366
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
2
Location
3575260
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.-109C>T
Allele
T
Clinical Significance
Likely benign