rs193214210
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
9
Location
110800910
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2532A>G (p.Ala844=)
Allele
G
Clinical Significance
Benign
A
G
9
110800910
SNP
NM_005592.4(MUSK):c.2532A>G (p.Ala844=)
G
Benign