rs2078078707
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110800638
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2260G>A (p.Asp754Asn)
Allele
A
Clinical Significance
Uncertain significance