rs77280560
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
2
Location
219235490
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.1708C>T (p.Pro570Ser)
Allele
T
Clinical Significance
Benign