rs1262405635
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
70124696
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006540.4(NCOA2):c.4086C>T (p.Gly1362=)
Allele
A
Clinical Significance
Likely benign