List of variants in gene SHANK2 reported as likely benign for autism, susceptiblity to

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_012309.5(SHANK2):c.4991T>C (p.Ile1664Thr)	rs150857128	0.00363
NM_012309.5(SHANK2):c.5025G>A (p.Thr1675=)	rs147288898	0.00020
NM_012309.5(SHANK2):c.4822G>A (p.Val1608Ile)	rs543988574	0.00013
NM_012309.5(SHANK2):c.451G>T (p.Asp151Tyr)	rs967203648	0.00010

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