ClinVar Miner

List of variants reported as uncertain significance for autism, susceptiblity to by Juno Genomics, Hangzhou Juno Genomics, Inc

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_018196.4(TMLHE):c.995+2T>C
NM_173495.3(PTCHD1):c.974A>G (p.Tyr325Cys)
NM_181332.3(NLGN4X):c.980T>A (p.Ile327Asn)

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