List of variants in gene GRIA3 reported as likely benign for syndromic intellectual disability

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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_007325.5(GRIA3):c.1181G>A (p.Arg394Gln)	rs138817389	0.00063
NM_007325.5(GRIA3):c.580G>A (p.Gly194Arg)	rs189437004	0.00009
NM_007325.5(GRIA3):c.466T>C (p.Tyr156His)	rs144902457	0.00005
NM_007325.5(GRIA3):c.1125T>C (p.Tyr375=)	rs562407134
NM_007325.5(GRIA3):c.123G>A (p.Met41Ile)
NM_007325.5(GRIA3):c.284C>T (p.Ser95Leu)

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