rs767794127
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
1
Location
930203
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.658C>T (p.Arg220Trp)
Allele
T
Clinical Significance
Uncertain significance