rs571312240
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
9
Location
110768047
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1148G>T (p.Ser383Ile)
Allele
T
Clinical Significance
Uncertain significance