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

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 13

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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.353A>C (p.Asp118Ala)	rs71524349	0.00279
NM_006005.3(WFS1):c.1554G>A (p.Met518Ile)	rs138232538	0.00202
NM_006005.3(WFS1):c.2052G>A (p.Ala684=)	rs71539668	0.00123
NM_006005.3(WFS1):c.966C>T (p.His322=)	rs140196582	0.00083
NM_006005.3(WFS1):c.2424C>T (p.Ser808=)	rs56035336	0.00048
NM_006005.3(WFS1):c.1760G>A (p.Arg587Gln)	rs71539657	0.00028
NM_006005.3(WFS1):c.1792G>A (p.Ala598Thr)	rs140125843	0.00022
NM_006005.3(WFS1):c.1758C>T (p.Ala586=)	rs145144527	0.00021
NM_006005.3(WFS1):c.2209G>A (p.Glu737Lys)	rs147834269	0.00018
NM_006005.3(WFS1):c.28C>T (p.Pro10Ser)	rs760256649	0.00006
NM_006005.3(WFS1):c.1134C>G (p.Thr378=)	rs71530904
NM_006005.3(WFS1):c.114C>T (p.Ser38=)	rs531593902

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