rs8135665
- not provided
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
38080269
Variant Type
SNP
Genes
LOC101927119
LOC105373027
Phenotypes
ClinVar
Name
NM_013356.3(SLC16A8):c.1198+571G>A
Allele
T
Clinical Significance
not provided