rs150205193
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
1
Location
939290
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1073C>T (p.Pro358Leu)
Allele
T
Clinical Significance
Uncertain significance