rs1060504495
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
1
Location
115732894
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.606+7A>T
Allele
A
Clinical Significance
Likely benign
T
A
1
115732894
SNP
NM_001232.4(CASQ2):c.606+7A>T
A
Likely benign