List of variants in gene GRIA3 reported as benign for X-linked syndromic intellectual disability

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000828.4(GRIA3):c.-2G=	rs58044961	1.00000
NM_007325.5(GRIA3):c.751-16T>C	rs550640	0.58620
NM_007325.5(GRIA3):c.1200T>C (p.Asn400=)	rs502434	0.57798
NM_007325.5(GRIA3):c.268+16757dup	rs778944548
NM_007325.5(GRIA3):c.268+16762dup	rs11452643
NM_007325.5(GRIA3):c.384dup (p.Phe129fs)	rs2147282654

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