Variants in gene WFS1 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.1672C>T (p.Arg558Cys)	rs199946797	0.00035
NM_006005.3(WFS1):c.2020G>A (p.Gly674Arg)	rs200672755	0.00016
NM_006005.3(WFS1):c.2171C>T (p.Pro724Leu)	rs28937890	0.00007
NM_006005.3(WFS1):c.1836G>A (p.Trp612Ter)	rs775158434	0.00006
NM_006005.3(WFS1):c.977C>T (p.Ala326Val)	rs369795224	0.00006
NM_006005.3(WFS1):c.2576G>A (p.Arg859Gln)	rs121912618	0.00002
NM_006005.3(WFS1):c.397G>A (p.Ala133Thr)	rs372249044	0.00001
NM_006005.3(WFS1):c.2096C>T (p.Thr699Met)	rs28937894
NM_006005.3(WFS1):c.911_914dup (p.Asp305_Met306insTer)	rs863224264

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