rs61753706
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
70156712
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006540.4(NCOA2):c.1653G>A (p.Ser551=)
Allele
T
Clinical Significance
Benign
C
T
8
70156712
SNP
NM_006540.4(NCOA2):c.1653G>A (p.Ser551=)
T
Benign