rs772619751
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
1
Location
115701291
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.1150A>G (p.Asn384Asp)
Allele
C
Clinical Significance
Uncertain significance