List of variants in gene WFS1 reported as uncertain significance for Nonsyndromic Hearing Loss, Dominant

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.366_369del	rs71537671	0.00032
NM_006005.3(WFS1):c.1290G>A (p.Ser430=)	rs752100338	0.00002
NM_006005.3(WFS1):c.356_357insTT	rs568320906
NM_006005.3(WFS1):c.*357CTTT[2]	rs373643818
NM_006005.3(WFS1):c.365_369del	rs886059535
NM_006005.3(WFS1):c.*683delinsTGGCTGTGGGGGA	rs886059540
NM_006005.3(WFS1):c.724_727del	rs71537674

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