List of variants in gene WRN reported as not provided for Werner syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000553.6(WRN):c.2500C>T (p.Arg834Cys)	rs3087425	0.00089
NM_000553.6(WRN):c.1105C>T (p.Arg369Ter)	rs17847577	0.00033
NM_000553.6(WRN):c.197C>T (p.Ser66Leu)	rs756575284	0.00004
NM_000553.6(WRN):c.3134A>G (p.Lys1045Arg)	rs369095273	0.00002
NM_000553.6(WRN):c.3094T>C (p.Ser1032Pro)	rs1802631623	0.00001
NM_000553.6(WRN):c.2089-3024A>G	rs281865157
NM_000553.6(WRN):c.2179dup (p.Cys727fs)	rs281865158
NM_000553.6(WRN):c.3139-1G>C	rs113993961
NM_000553.6(WRN):c.3460-2A>C	rs281865159
NM_000553.6(WRN):c.3590del (p.Asn1197fs)	rs281865160

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