rs369803898
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
1
Location
939103
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1031A>C (p.Lys344Thr)
Allele
C
Clinical Significance
Uncertain significance