List of variants in gene DICER1 reported as pathogenic by ClinGen DICER1 and miRNA-Processing Gene Variant Curation Expert Panel, ClinGen

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.1408G>T (p.Glu470Ter)	rs886037671
NM_177438.3(DICER1):c.1880_1883del (p.Ile627fs)	rs886037680
NM_177438.3(DICER1):c.1907+1G>A	rs1131691217
NM_177438.3(DICER1):c.2650+1G>T	rs886037691
NM_177438.3(DICER1):c.2988-1G>T	rs1131691192
NM_177438.3(DICER1):c.3019C>T (p.Gln1007Ter)	rs1131691189
NM_177438.3(DICER1):c.5096-12G>A	rs1566750865
NM_177438.3(DICER1):c.5104C>T (p.Gln1702Ter)	rs886037723
NM_177438.3(DICER1):c.5113G>A (p.Glu1705Lys)	rs1890101390
NM_177438.3(DICER1):c.5125G>A (p.Asp1709Asn)	rs1595331264
NM_177438.3(DICER1):c.5425G>A (p.Gly1809Arg)	rs1595314951
NM_177438.3(DICER1):c.5428G>T (p.Asp1810Tyr)	rs775912475
NM_177438.3(DICER1):c.5441C>T (p.Ser1814Leu)	rs1060503625
NM_177438.3(DICER1):c.5479del (p.Leu1827fs)	rs1555366197
NM_177438.3(DICER1):c.878_881del (p.Arg293fs)	rs886037733

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