NM_000036.2(AMPD1):c.702T>A (p.Pro234=) AND Autistic disorder of childhood onset
| Significance: | Likely benign |
|---|---|
| ClinVar: | RCV000143854 |
Variant: NM_000036.2(AMPD1):c.702T>A (p.Pro234=) |
|
| Type: | Variant |
Allele: NM_000036.2(AMPD1):c.702T>A (p.Pro234=) 97356 |
|
| Gene: | AMPD1 |
| Type: | single nucleotide variant |
| Location: |
Chr1: 114680423
- assembly
GRCh38 Chr1: 115223044 - assembly GRCh37 |
| References: | dbSNP:
587779377 |
Condition |
|
| Disease: | Autistic disorder of childhood onset |