rs863223356
- Likely pathogenic
Your Genotype
Sign InDescription
COS with Asperger's Disorder
Reference Allele
A
Alternative Allele
G
Chromosome
11
Location
65661693
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.329T>C (p.Ile110Thr)
Allele
G
Clinical Significance
Likely pathogenic