List of variants in gene SHANK2 reported as likely benign by GeneDx

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_012309.5(SHANK2):c.1371C>T (p.Pro457=)	rs782397098	0.00025
NM_012309.5(SHANK2):c.4986G>A (p.Pro1662=)	rs139247945	0.00014
NM_012309.5(SHANK2):c.2001C>T (p.Ser667=)	rs199845489	0.00011
NM_012309.5(SHANK2):c.2403C>T (p.Pro801=)	rs781966470	0.00002
NM_012309.5(SHANK2):c.412-9C>T	rs201663845	0.00002
NM_012309.5(SHANK2):c.1401C>T (p.Tyr467=)	rs782545722	0.00001
NM_012309.5(SHANK2):c.3042G>A (p.Val1014=)	rs781874756	0.00001
NM_012309.5(SHANK2):c.2421G>C (p.Pro807=)	rs782015393
NM_012309.5(SHANK2):c.3231C>A (p.Pro1077=)	rs1591489781
NM_012309.5(SHANK2):c.4125C>T (p.Ile1375=)	rs1218363195

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