List of variants in gene DRAM2 reported as uncertain significance for perceptual disorders

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001349884.2(DRAM2):c.737T>C (p.Leu246Pro)	rs148031211	0.00032
NM_001349884.2(DRAM2):c.719A>G (p.Asn240Ser)	rs761405900	0.00003
NM_001349884.2(DRAM2):c.89C>T (p.Ala30Val)	rs147979228	0.00002
NM_001349884.2(DRAM2):c.246T>G (p.Ser82Arg)	rs772262465	0.00001

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