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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:
Type: single nucleotide variant
Location: Chr1: 114680423 - assembly GRCh38
Chr1: 115223044 - assembly GRCh37
References: dbSNP: 587779377

Condition

Disease: Autistic disorder of childhood onset