rs150567570
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
19
Location
7640769
Variant Type
SNP
Genes
ClinVar
Name
NM_006949.4(STXBP2):c.285G>A (p.Pro95=)
Allele
A
Clinical Significance
Likely benign