rs61747683
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
2
Location
219233429
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.815A>G (p.Tyr272Cys)
Allele
G
Clinical Significance
Benign