rs187455529
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
38078399
Variant Type
SNP
Genes
LOC105373027
Phenotypes
ClinVar
Name
NM_013356.3(SLC16A8):c.1504G>A (p.Glu502Lys)
Allele
T
Clinical Significance
Benign