rs1570831633
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
1
Location
115738321
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.435A>G (p.Pro145=)
Allele
C
Clinical Significance
Likely benign