rs41279057
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110941779
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001351411.2(LPAR1):c.435G>A (p.Glu145=)
Allele
T
Clinical Significance
Benign