rs370094071
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
9
Location
110800977
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2599G>T (p.Val867Leu)
Allele
T
Clinical Significance
Benign
G
T
9
110800977
SNP
NM_005592.4(MUSK):c.2599G>T (p.Val867Leu)
T
Benign