rs1319203200
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
9
Location
110762204
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.916T>G (p.Trp306Gly)
Allele
G
Clinical Significance
Uncertain significance