rs2077193041
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
110747735
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.848T>C (p.Ile283Thr)
Allele
C
Clinical Significance
Uncertain significance