List of variants in gene FASN reported as uncertain significance for not provided

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004104.5(FASN):c.3829C>G (p.Pro1277Ala)	rs764159372	0.00021
NM_004104.5(FASN):c.1837G>A (p.Ala613Thr)	rs201599253	0.00014
NM_004104.5(FASN):c.1468C>T (p.Arg490Cys)	rs533081221	0.00007
NM_004104.5(FASN):c.4633C>T (p.Arg1545Cys)	rs150970220	0.00005
NM_004104.5(FASN):c.1740C>T (p.His580=)	rs746029897	0.00003
NM_004104.5(FASN):c.2881T>C (p.Trp961Arg)	rs763326290	0.00002
NM_004104.5(FASN):c.3302C>T (p.Ser1101Leu)	rs143739434	0.00002
NM_004104.5(FASN):c.2035G>A (p.Gly679Ser)	rs747822458	0.00001
NM_004104.5(FASN):c.5113C>T (p.Arg1705Trp)	rs766947051	0.00001
NM_004104.5(FASN):c.3815C>T (p.Ala1272Val)
NM_004104.5(FASN):c.4409+1G>A
NM_004104.5(FASN):c.4447G>C (p.Val1483Leu)
NM_004104.5(FASN):c.4994T>C (p.Val1665Ala)	rs2144787060
NM_004104.5(FASN):c.5407A>G (p.Ser1803Gly)	rs2144785472
NM_004104.5(FASN):c.6818G>A (p.Cys2273Tyr)

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