rs764498089
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
3580131
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.378C>T (p.His126=)
Allele
T
Clinical Significance
Likely benign