ClinVar Miner

List of variants reported as likely benign for language disorder

Included ClinVar conditions (10):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_007347.5(AP4E1):c.542+11T>G	rs58882998	0.00762
NM_024795.4(TM4SF20):c.559A>G (p.Ile187Val)	rs575973865	0.00006
NM_001197104.2(KMT2A):c.2633G>A (p.Arg878Gln)	rs879253756	0.00001

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