rs201616041
- Likely benign
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
9
Location
110800460
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2082C>T (p.Pro694=)
Allele
T
Clinical Significance
Likely benign
Name
NM_005592.4(MUSK):c.2082C>A (p.Pro694=)
Allele
A
Clinical Significance
Likely benign