List of variants in gene GLRA2 reported as pathogenic for 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002063.4(GLRA2):c.407A>G (p.Asn136Ser)	rs1276905604	0.00001
NM_002063.4(GLRA2):c.754C>T (p.Arg252Cys)	rs748764171	0.00001
NC_000023.10:g.14693216_14836199del
NM_002063.4(GLRA2):c.458G>A (p.Arg153Gln)	rs2147065620
NM_002063.4(GLRA2):c.887C>T (p.Thr296Met)	rs1601761445

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