List of variants in gene WFS1 reported as likely risk allele for Wolfram syndrome 1

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.577A>C (p.Lys193Gln)	rs41264699	0.00267
NM_006005.3(WFS1):c.1195T>G (p.Trp399Gly)	rs767561828	0.00010
NM_006005.3(WFS1):c.232G>A (p.Gly78Arg)	rs777964510	0.00003
NM_006005.3(WFS1):c.1015G>A (p.Asp339Asn)	rs772392224	0.00002
NM_006005.3(WFS1):c.1099G>T (p.Asp367Tyr)	rs886059528	0.00002
NM_006005.3(WFS1):c.2453G>A (p.Arg818His)	rs575851859	0.00002
NM_006005.3(WFS1):c.2470G>A (p.Glu824Lys)	rs367547063	0.00002
NM_006005.3(WFS1):c.412C>T (p.Arg138Cys)	rs780394696	0.00002
NM_006005.3(WFS1):c.2263T>C (p.Cys755Arg)	rs797045075	0.00001
NM_006005.3(WFS1):c.2455C>G (p.Gln819Glu)	rs104893881	0.00001
NM_006005.3(WFS1):c.1046TCT[1] (p.Phe350del)	rs1560418164
NM_006005.3(WFS1):c.1607T>A (p.Val536Glu)	rs1553878625
NM_006005.3(WFS1):c.1613T>C (p.Phe538Ser)	rs1560419651
NM_006005.3(WFS1):c.1684G>C (p.Gly562Arg)	rs753237278
NM_006005.3(WFS1):c.2061G>T (p.Gln687His)	rs760938537
NM_006005.3(WFS1):c.2201T>A (p.Leu734His)	rs1409267086
NM_006005.3(WFS1):c.2293T>C (p.Cys765Arg)	rs727503752
NM_006005.3(WFS1):c.2323T>G (p.Phe775Val)	rs727503753
NM_006005.3(WFS1):c.2369C>G (p.Ser790Trp)	rs369107336
NM_006005.3(WFS1):c.2405T>C (p.Ile802Thr)	rs1730963697
NM_006005.3(WFS1):c.2430C>G (p.Phe810Leu)	rs1553879021
NM_006005.3(WFS1):c.2459G>T (p.Gly820Val)	rs764842865
NM_006005.3(WFS1):c.2477G>A (p.Ser826Asn)	rs1730968028
NM_006005.3(WFS1):c.436C>T (p.Arg146Cys)	rs1553876694
NM_006005.3(WFS1):c.529C>T (p.Arg177Cys)	rs760631912
NM_006005.3(WFS1):c.754A>G (p.Lys252Glu)	rs1553877330
NM_006005.3(WFS1):c.901G>A (p.Glu301Lys)	rs1560417758

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