rs375406874
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
9
Location
110800302
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.1928-4C>A
Allele
A
Clinical Significance
Likely benign
C
A
T
9
110800302
SNP
NM_005592.4(MUSK):c.1928-4C>A
A
Likely benign