List of variants in gene DICER1 reported as not provided for not specified

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.5095+13C>T	rs116247322	0.00577
NM_177438.3(DICER1):c.2557A>G (p.Ile853Val)	rs61729795	0.00252
NM_177438.3(DICER1):c.1825G>T (p.Asp609Tyr)	rs114947750	0.00180
NM_177438.3(DICER1):c.20A>G (p.Gln7Arg)	rs117358479	0.00165
NM_177438.3(DICER1):c.2614G>A (p.Ala872Thr)	rs149242330	0.00074
NM_177438.3(DICER1):c.59C>T (p.Ala20Val)	rs147660793	0.00070
NM_177438.3(DICER1):c.4923T>G (p.Cys1641Trp)	rs587778231	0.00021
NM_177438.3(DICER1):c.3553G>A (p.Ala1185Thr)	rs150514959	0.00016
NM_177438.3(DICER1):c.1013A>C (p.Glu338Ala)	rs587778232	0.00008
NM_177438.3(DICER1):c.179C>T (p.Thr60Ile)	rs587778228	0.00007
NM_177438.3(DICER1):c.5276A>G (p.Lys1759Arg)	rs144259142	0.00007
NM_177438.3(DICER1):c.3334A>G (p.Asn1112Asp)	rs587778229	0.00002
NM_177438.3(DICER1):c.5516G>A (p.Arg1839Gln)	rs587778233	0.00002
NM_177438.3(DICER1):c.4254GGA[2] (p.Glu1420del)	rs544960260
NM_177438.3(DICER1):c.4795C>T (p.Arg1599Trp)	rs587778230
NM_177438.3(DICER1):c.56C>T (p.Pro19Leu)	rs587778227

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