rs73077102
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
2
Location
219237136
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001286423.2(GLB1L):c.1901A>G (p.His634Arg)
Allele
C
Clinical Significance
Benign