rs1006838420
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
3575878
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.137C>T (p.Thr46Met)
Allele
T
Clinical Significance
Uncertain significance