rs201791900
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
9
Location
110767956
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1057C>A (p.His353Asn)
Allele
A
Clinical Significance
Likely benign