List of variants reported as likely benign for obsolete DICER1 syndrome by Illumina Laboratory Services, Illumina

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.4891T>G (p.Ser1631Ala)	rs145551486	0.00128
NM_177438.3(DICER1):c.5145C>T (p.Leu1715=)	rs139500905	0.00121
NM_177438.3(DICER1):c.4802A>T (p.Lys1601Met)	rs181018393	0.00012
NM_177438.3(DICER1):c.5527+7T>A	rs375239471	0.00009
NM_177438.3(DICER1):c.*5G>A	rs770907156	0.00006
NM_177438.3(DICER1):c.3674A>G (p.Tyr1225Cys)	rs146584765	0.00006
NM_177438.3(DICER1):c.5738A>G (p.Lys1913Arg)	rs752116341	0.00006
NM_177438.3(DICER1):c.1691C>T (p.Ala564Val)	rs201298288	0.00005
NM_177438.3(DICER1):c.2872A>G (p.Ser958Gly)	rs752905540	0.00005
NM_177438.3(DICER1):c.3422C>T (p.Ser1141Phe)	rs780815020	0.00004
NM_177438.3(DICER1):c.3334A>G (p.Asn1112Asp)	rs587778229	0.00002
NM_177438.3(DICER1):c.3777C>T (p.Ala1259=)	rs770390974	0.00002
NM_177438.3(DICER1):c.4199A>G (p.Asp1400Gly)	rs139536688	0.00002
NM_177438.3(DICER1):c.2496G>C (p.Lys832Asn)	rs769292296	0.00001
NM_177438.3(DICER1):c.5217G>C (p.Leu1739=)	rs774703353	0.00001

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