List of variants in gene DICER1 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.2370G>A (p.Arg790=)	rs112712209	0.00777
NM_177438.3(DICER1):c.1377-4T>G	rs192490028	0.00240
NM_177438.3(DICER1):c.4891T>G (p.Ser1631Ala)	rs145551486	0.00128
NM_177438.3(DICER1):c.1908-4A>G	rs112284114	0.00123
NM_177438.3(DICER1):c.3213A>G (p.Arg1071=)	rs148959399	0.00123
NM_177438.3(DICER1):c.5604-12G>A	rs149841885	0.00122
NM_177438.3(DICER1):c.4923T>G (p.Cys1641Trp)	rs587778231	0.00021
NM_177438.3(DICER1):c.5738A>G (p.Lys1913Arg)	rs752116341	0.00006
NM_177438.3(DICER1):c.359A>T (p.Lys120Met)	rs1060503608	0.00003
NM_177438.3(DICER1):c.1377-18T>A	rs1032236740	0.00002
NM_177438.3(DICER1):c.4449G>A (p.Met1483Ile)	rs1454569806	0.00002
NM_177438.3(DICER1):c.4475T>C (p.Met1492Thr)	rs370947079	0.00002
NM_177438.3(DICER1):c.1770T>C (p.Cys590=)	rs777355058	0.00001
NM_177438.3(DICER1):c.2536A>G (p.Ile846Val)	rs201212908	0.00001
NM_177438.3(DICER1):c.3269+12C>T	rs775380766	0.00001
NM_177438.3(DICER1):c.3578A>G (p.Asn1193Ser)	rs1288723916	0.00001
NM_177438.3(DICER1):c.3722A>G (p.Lys1241Arg)	rs764415288	0.00001
NM_177438.3(DICER1):c.920G>A (p.Arg307His)	rs149718671	0.00001
NM_177438.3(DICER1):c.1510-4del	rs546524688
NM_177438.3(DICER1):c.1966C>T (p.Arg656Ter)	rs754081635
NM_177438.3(DICER1):c.2210C>T (p.Pro737Leu)	rs1595391071
NM_177438.3(DICER1):c.2494A>G (p.Lys832Glu)	rs1060503613
NM_177438.3(DICER1):c.3890T>C (p.Ile1297Thr)	rs761578934
NM_177438.3(DICER1):c.4608T>C (p.Gly1536=)	rs1890331241
NM_177438.3(DICER1):c.5171C>T (p.Pro1724Leu)	rs749900564
NM_177438.3(DICER1):c.5441C>T (p.Ser1814Leu)	rs1060503625

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