List of variants in gene WFS1 reported as 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.1805C>T (p.Ala602Val)	rs2230720	0.02889
NM_006005.3(WFS1):c.1726G>A (p.Gly576Ser)	rs1805069	0.01068
NM_006005.3(WFS1):c.1495C>T (p.Leu499Phe)	rs114152068	0.00810
NM_006005.3(WFS1):c.2611G>A (p.Val871Met)	rs71532874	0.00761
NM_006005.3(WFS1):c.2335G>A (p.Val779Met)	rs141328044	0.00672
NM_006005.3(WFS1):c.1675G>A (p.Ala559Thr)	rs55814513	0.00396
NM_006005.3(WFS1):c.917T>C (p.Met306Thr)	rs146114074	0.00389
NM_006005.3(WFS1):c.2327A>T (p.Glu776Val)	rs56002719	0.00354
NM_006005.3(WFS1):c.353A>C (p.Asp118Ala)	rs71524349	0.00279
NM_006005.3(WFS1):c.577A>C (p.Lys193Gln)	rs41264699	0.00249
NM_006005.3(WFS1):c.2356G>A (p.Gly786Ser)	rs71578980	0.00239
NM_006005.3(WFS1):c.2012C>T (p.Ala671Val)	rs71530907	0.00021
NM_006005.3(WFS1):c.2158A>G (p.Ile720Val)	rs1805070
NM_006005.3(WFS1):c.350C>T (p.Thr117Met)	rs141225426

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