List of variants in gene DICER1 reported as likely benign by Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.2997T>G (p.Leu999=)	rs12018992	0.01764
NM_177438.3(DICER1):c.1377-4T>G	rs192490028	0.00240
NM_177438.3(DICER1):c.485G>A (p.Gly162Asp)	rs142815547	0.00218
NM_177438.3(DICER1):c.20A>G (p.Gln7Arg)	rs117358479	0.00165
NM_177438.3(DICER1):c.5145C>T (p.Leu1715=)	rs139500905	0.00121
NM_177438.3(DICER1):c.4014G>A (p.Ala1338=)	rs143454689	0.00099
NM_177438.3(DICER1):c.2614G>A (p.Ala872Thr)	rs149242330	0.00074
NM_177438.3(DICER1):c.2040+29T>C	rs370866625	0.00015
NM_177438.3(DICER1):c.4616C>T (p.Thr1539Met)	rs747901058	0.00013
NM_177438.3(DICER1):c.4740G>T (p.Gln1580His)	rs369465519	0.00003
NM_177438.3(DICER1):c.184G>A (p.Val62Ile)	rs746671039	0.00002
NM_177438.3(DICER1):c.3334A>G (p.Asn1112Asp)	rs587778229	0.00002
NM_177438.3(DICER1):c.4199A>G (p.Asp1400Gly)	rs139536688	0.00002
NM_177438.3(DICER1):c.255C>G (p.Ile85Met)	rs763422772	0.00001
NM_177438.3(DICER1):c.4888C>T (p.Arg1630Cys)	rs549532374	0.00001
NM_177438.3(DICER1):c.5330T>A (p.Leu1777His)	rs780545199	0.00001
NM_177438.3(DICER1):c.884C>G (p.Ser295Cys)	rs548231008	0.00001
NM_177438.3(DICER1):c.1410G>A (p.Glu470=)	rs774271782
NM_177438.3(DICER1):c.2040+54dup	rs141723381
NM_177438.3(DICER1):c.2830C>A (p.Arg944=)	rs137852978
NM_177438.3(DICER1):c.3328A>G (p.Ile1110Val)	rs1566769439
NM_177438.3(DICER1):c.3649T>A (p.Tyr1217Asn)	rs1891127892
NM_177438.3(DICER1):c.4420A>G (p.Thr1474Ala)	rs1890354220
NM_177438.3(DICER1):c.4806C>T (p.Ala1602=)	rs1890302137
NM_177438.3(DICER1):c.5133T>G (p.Ile1711Met)	rs1890097799

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