rs72554062
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
1
Location
115738265
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.491A>G (p.Tyr164Cys)
Allele
C
Clinical Significance
Uncertain significance