ClinVar Miner

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

Included ClinVar conditions (163):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_001256743.1(GRIA3):c.380dupG (p.Gly128Trpfs) rs778944548

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