rs751266636
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
9
Location
110775882
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1279C>G (p.His427Asp)
Allele
G
Clinical Significance
Uncertain significance