List of variants in gene POU1F1 reported as uncertain significance for not provided

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_000306.4(POU1F1):c.370A>G (p.Met124Val)	rs143373007	0.00183
NM_000306.4(POU1F1):c.252C>T (p.His84=)	rs4988460	0.00098
NM_000306.4(POU1F1):c.605-5T>G	rs201406891	0.00065
NM_000306.4(POU1F1):c.27T>C (p.Ala9=)	rs35560664	0.00022
NM_000306.4(POU1F1):c.40C>G (p.Pro14Ala)	rs200873915	0.00013
NM_000306.4(POU1F1):c.699T>C (p.Phe233=)	rs1418782481	0.00003
NM_000306.4(POU1F1):c.104T>C (p.Leu35Pro)	rs558209279	0.00001
NM_000306.4(POU1F1):c.143-2A>G	rs746709336	0.00001
NM_000306.4(POU1F1):c.301G>A (p.Asp101Asn)	rs976923764	0.00001
NM_000306.4(POU1F1):c.649C>T (p.Arg217Ter)	rs761275346	0.00001
NM_000306.4(POU1F1):c.106_107delinsGT (p.Pro36Val)	rs2106944034
NM_000306.4(POU1F1):c.209T>C (p.Met70Thr)
NM_000306.4(POU1F1):c.439+5G>A
NM_000306.4(POU1F1):c.666-8C>G	rs182127067
NM_000306.4(POU1F1):c.671C>T (p.Ala224Val)	rs2106925411
NM_000306.4(POU1F1):c.698T>C (p.Phe233Ser)
NM_000306.4(POU1F1):c.770T>C (p.Val257Ala)
NM_000306.4(POU1F1):c.797G>C (p.Arg266Thr)	rs1553674729
NM_000306.4(POU1F1):c.811C>T (p.Arg271Trp)	rs104893755
NM_000306.4(POU1F1):c.824G>A (p.Ser275Asn)

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