rs1599386139
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
19
Location
7637154
Variant Type
SNP
ClinVar
Name
NM_006949.4(STXBP2):c.5C>T (p.Ala2Val)
Allele
T
Clinical Significance
Uncertain significance