ClinVar Miner

List of variants in gene SHANK3 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001372044.2(SHANK3):c.3597C>G (p.Pro1199=)	rs1377079422
NM_001372044.2(SHANK3):c.4613dup (p.Arg1539fs)	rs2518430356

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