rs751972431
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
9
Location
110775833
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1230G>C (p.Trp410Cys)
Allele
C
Clinical Significance
Uncertain significance