List of variants in gene WHRN reported as likely benign 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_015404.4(WHRN):c.1515G>A (p.Ala505=)	rs34252199	0.03118
NM_015404.4(WHRN):c.-257C>G	rs73555447	0.02919
NM_015404.4(WHRN):c.-295C>G	rs7861589	0.01478
NM_015404.4(WHRN):c.1166+18G>A	rs149202009	0.00456
NM_015404.4(WHRN):c.2586C>A (p.His862Gln)	rs117592152	0.00424
NM_015404.4(WHRN):c.1352G>A (p.Gly451Asp)	rs117352600	0.00120
NM_015404.4(WHRN):c.1349G>A (p.Arg450His)	rs200377723	0.00007
NM_015404.4(WHRN):c.2307C>T (p.Gly769=)	rs148971049	0.00006
NM_015404.4(WHRN):c.-314C>T	rs57258861
NM_015404.4(WHRN):c.-608_-601del	rs150944893

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