ClinVar Miner

List of variants reported as uncertain significance for autism, susceptiblity to by Johns Hopkins Genomics, Johns Hopkins University

Included ClinVar conditions (22):

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_001170629.2(CHD8):c.4285C>T (p.Arg1429Trp)	rs780639697	0.00002
NM_012309.5(SHANK2):c.3266G>A (p.Arg1089His)	rs781863842
NM_181332.3(NLGN4X):c.2428G>A (p.Gly810Arg)	rs1181689310

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