rs57521028
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
19
Location
7610597
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020902.2(CAMSAP3):c.882C>T (p.Tyr294=)
Allele
T
Clinical Significance
Benign
C
T
19
7610597
SNP
NM_020902.2(CAMSAP3):c.882C>T (p.Tyr294=)
T
Benign