rs2077898016
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
9
Location
110787695
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1784C>G (p.Pro595Arg)
Allele
G
Clinical Significance
Uncertain significance