rs1554757237
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110800735
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2357G>A (p.Trp786Ter)
Allele
A
Clinical Significance
Likely pathogenic