List of variants in gene WFS1 reported as likely benign by Personalized Diabetes Medicine Program, University of Maryland School of Medicine

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.2596G>A (p.Asp866Asn)	rs3821945	0.00185
NM_006005.3(WFS1):c.1277G>A (p.Cys426Tyr)	rs35218685	0.00160
NM_006005.3(WFS1):c.1597C>T (p.Pro533Ser)	rs146132083	0.00076
NM_006005.3(WFS1):c.2233G>A (p.Gly745Ser)	rs139185707	0.00068
NM_006005.3(WFS1):c.1153G>A (p.Glu385Lys)	rs71524353	0.00057
NM_006005.3(WFS1):c.1760G>A (p.Arg587Gln)	rs71539657	0.00028
NM_006005.3(WFS1):c.2563T>C (p.Ser855Pro)	rs141833472	0.00021

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