rs202239254
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
9
Location
110775963
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1360G>A (p.Asp454Asn)
Allele
A
Clinical Significance
Uncertain significance