rs115507207
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
8
Location
70733849
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011720.2(XKR9):c.547C>T (p.Gln183Ter)
Allele
T
Clinical Significance
Benign