rs1000750610
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
1
Location
942424
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1489C>T (p.Pro497Ser)
Allele
T
Clinical Significance
Uncertain significance