rs1362882035
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
1
Location
942762
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1757C>T (p.Pro586Leu)
Allele
T
Clinical Significance
Uncertain significance