rs188395735
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
38082672
Variant Type
SNP
Genes
LOC101927119
Phenotypes
ClinVar
Name
NM_013356.3(SLC16A8):c.202C>T (p.Leu68Phe)
Allele
A
Clinical Significance
Benign