rs772683882
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110800400
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.2022C>T (p.Thr674=)
Allele
T
Clinical Significance
Likely benign