rs115177449
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
70128911
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006540.4(NCOA2):c.3394G>A (p.Val1132Ile)
Allele
T
Clinical Significance
Likely benign