rs375122052
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
1
Location
935847
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.918C>G (p.Ser306Arg)
Allele
G
Clinical Significance
Uncertain significance