rs928134595
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
9
Location
110785553
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1613C>G (p.Thr538Arg)
Allele
G
Clinical Significance
Uncertain significance