rs756140787
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
1
Location
935819
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.890G>T (p.Arg297Leu)
Allele
T
Clinical Significance
Uncertain significance