ClinVar Miner

List of variants in gene ASH1L reported as likely benign for Syndromic complex neurodevelopmental disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_018489.3(ASH1L):c.851C>T (p.Thr284Ile)	rs138738661	0.00006
NM_018489.3(ASH1L):c.1589C>T (p.Pro530Leu)	rs764247635	0.00003

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