rs1038479586
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
9
Location
110767999
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1100G>C (p.Arg367Pro)
Allele
C
Clinical Significance
Uncertain significance
Name
NM_005592.4(MUSK):c.1100G>A (p.Arg367Gln)
Allele
A
Clinical Significance
Uncertain significance