rs115949101
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
2
Location
219234191
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.1107A>C (p.Val369=)
Allele
C
Clinical Significance
Benign