rs115239774
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
19
Location
7639112
Variant Type
SNP
Genes
ClinVar
Name
NM_006949.4(STXBP2):c.169+12C>T
Allele
T
Clinical Significance
Benign
C
G
T
19
7639112
SNP
NM_006949.4(STXBP2):c.169+12C>T
T
Benign