List of variants in gene WFS1 reported as likely benign by Eurofins NTD LLC (GA)

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_006005.3(WFS1):c.2452C>T (p.Arg818Cys)	rs35932623	0.00390
NM_006005.3(WFS1):c.482G>A (p.Arg161Gln)	rs115346085	0.00204
NM_006005.3(WFS1):c.1554G>A (p.Met518Ile)	rs138232538	0.00202
NM_006005.3(WFS1):c.227G>T (p.Gly76Val)	rs200135768	0.00197
NM_006005.3(WFS1):c.2052G>A (p.Ala684=)	rs71539668	0.00123
NM_006005.3(WFS1):c.1143G>A (p.Leu381=)	rs151153967	0.00078
NM_006005.3(WFS1):c.2233G>A (p.Gly745Ser)	rs139185707	0.00068
NM_006005.3(WFS1):c.1779G>C (p.Glu593Asp)	rs144783536	0.00063
NM_006005.3(WFS1):c.1792G>A (p.Ala598Thr)	rs140125843	0.00022
NM_006005.3(WFS1):c.114C>T (p.Ser38=)	rs531593902

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