rs3811003
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
1
Location
115705169
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001232.4(CASQ2):c.939+23C>T
Allele
A
Clinical Significance
Benign
G
A
C
1
115705169
SNP
NM_001232.4(CASQ2):c.939+23C>T
A
Benign