rs61732234
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
3575840
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.99C>T (p.Asn33=)
Allele
T
Clinical Significance
Benign
C
T
2
3575840
SNP
NM_001011.4(RPS7):c.99C>T (p.Asn33=)
T
Benign