rs149677938
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
1
Location
939076
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1004G>T (p.Arg335Leu)
Allele
T
Clinical Significance
Uncertain significance