rs751889864
- Likely pathogenic
Your Genotype
Sign InDescription
This variant was classified as: Likely pathogenic.
Reference Allele
T
Alternative Allele
A
C
Chromosome
9
Location
110785664
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1724T>C (p.Ile575Thr)
Allele
C
Clinical Significance
Likely pathogenic