rs61753707
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
8
Location
70216728
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006540.4(NCOA2):c.18A>G (p.Glu6=)
Allele
C
Clinical Significance
Benign
T
C
8
70216728
SNP
NM_006540.4(NCOA2):c.18A>G (p.Glu6=)
C
Benign