rs1585905814
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
8
Location
70162841
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006540.4(NCOA2):c.846T>G (p.Ser282=)
Allele
C
Clinical Significance
Likely benign