List of variants in gene WFS1 reported as benign by Eurofins NTD LLC (GA)

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.997G>A (p.Val333Ile)	rs1801212	0.80149
NM_006005.3(WFS1):c.*47T>C	rs1046317	0.71708
NM_006005.3(WFS1):c.2565A>G (p.Ser855=)	rs1046316	0.70506
NM_006005.3(WFS1):c.684C>G (p.Arg228=)	rs1801213	0.68223
NM_006005.3(WFS1):c.1500C>T (p.Asn500=)	rs1801214	0.63787
NM_006005.3(WFS1):c.461-9A>G	rs10010131	0.63169
NM_006005.3(WFS1):c.461-15C>T	rs9998519	0.62200
NM_006005.3(WFS1):c.2433G>A (p.Lys811=)	rs1046314	0.57941
NM_006005.3(WFS1):c.1185C>T (p.Val395=)	rs1801206	0.56648
NM_006005.3(WFS1):c.1832G>A (p.Arg611His)	rs734312	0.43085
NM_006005.3(WFS1):c.2322G>A (p.Lys774=)	rs2230721	0.06809
NM_006005.3(WFS1):c.1367G>A (p.Arg456His)	rs1801208	0.04977
NM_006005.3(WFS1):c.1023C>T (p.Phe341=)	rs56072215	0.04932
NM_006005.3(WFS1):c.1805C>T (p.Ala602Val)	rs2230720	0.02889
NM_006005.3(WFS1):c.9C>T (p.Ser3=)	rs71524363	0.01435
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.2205C>T (p.Tyr735=)	rs71530911	0.00274
NM_006005.3(WFS1):c.1674C>T (p.Arg558=)	rs61735402	0.00269
NM_006005.3(WFS1):c.2356G>A (p.Gly786Ser)	rs71578980	0.00239
NM_006005.3(WFS1):c.2124C>T (p.Arg708=)	rs61735401	0.00223
NM_006005.3(WFS1):c.712+16G>A	rs71524367	0.00213
NM_006005.3(WFS1):c.2596G>A (p.Asp866Asn)	rs3821945	0.00185
NM_006005.3(WFS1):c.1294C>G (p.Leu432Val)	rs35031397
NM_006005.3(WFS1):c.1725C>T (p.Ala575=)	rs2230719
NM_006005.3(WFS1):c.2158A>G (p.Ile720Val)	rs1805070
NM_006005.3(WFS1):c.2370G>A (p.Ser790=)	rs150936382

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