List of variants in gene WFS1 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.1495C>T (p.Leu499Phe)	rs114152068	0.00810
NM_006005.3(WFS1):c.1308C>T (p.Thr436=)	rs71539646	0.00773
NM_006005.3(WFS1):c.2452C>T (p.Arg818Cys)	rs35932623	0.00390
NM_006005.3(WFS1):c.577A>C (p.Lys193Gln)	rs41264699	0.00249
NM_006005.3(WFS1):c.2596G>A (p.Asp866Asn)	rs3821945	0.00185
NM_006005.3(WFS1):c.2012C>T (p.Ala671Val)	rs71530907	0.00021

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