ClinVar Miner

List of variants in gene GRIN2D reported as pathogenic for not provided

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000836.4(GRIN2D):c.2024C>A (p.Ala675Asp)	rs1600982197
NM_000836.4(GRIN2D):c.2041A>G (p.Met681Val)	rs1555893359

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