List of variants in gene DICER1 reported as uncertain significance for DICER1-related disorder

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: 43

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.4923T>G (p.Cys1641Trp)	rs587778231	0.00019
NM_177438.3(DICER1):c.3475G>C (p.Glu1159Gln)	rs145693584	0.00010
NM_177438.3(DICER1):c.3773T>C (p.Met1258Thr)	rs144095207	0.00010
NM_177438.3(DICER1):c.4406T>C (p.Leu1469Pro)	rs200890670	0.00010
NM_177438.3(DICER1):c.4870G>C (p.Ala1624Pro)	rs372967646	0.00010
NM_177438.3(DICER1):c.179C>T (p.Thr60Ile)	rs587778228	0.00007
NM_177438.3(DICER1):c.2720T>C (p.Ile907Thr)	rs200408568	0.00006
NM_177438.3(DICER1):c.1410G>C (p.Glu470Asp)	rs774271782	0.00004
NM_177438.3(DICER1):c.1582A>G (p.Ile528Val)	rs755649018	0.00004
NM_177438.3(DICER1):c.1795A>G (p.Thr599Ala)	rs766492523	0.00003
NM_177438.3(DICER1):c.1877C>A (p.Thr626Lys)	rs375579739	0.00003
NM_177438.3(DICER1):c.1883A>G (p.Asn628Ser)	rs756051157	0.00003
NM_177438.3(DICER1):c.3823A>G (p.Met1275Val)	rs751764482	0.00003
NM_177438.3(DICER1):c.5471G>T (p.Gly1824Val)	rs377685186	0.00003
NM_177438.3(DICER1):c.4199A>G (p.Asp1400Gly)	rs139536688	0.00002
NM_177438.3(DICER1):c.4475T>C (p.Met1492Thr)	rs370947079	0.00002
NM_177438.3(DICER1):c.773G>T (p.Gly258Val)	rs188327838	0.00002
NM_177438.3(DICER1):c.1469G>A (p.Arg490His)	rs1006363970	0.00001
NM_177438.3(DICER1):c.1955A>C (p.Lys652Thr)	rs755150419	0.00001
NM_177438.3(DICER1):c.2390A>G (p.Asp797Gly)	rs755375348	0.00001
NM_177438.3(DICER1):c.2476A>G (p.Thr826Ala)	rs1328529319	0.00001
NM_177438.3(DICER1):c.263A>T (p.Asp88Val)	rs775828379	0.00001
NM_177438.3(DICER1):c.2738A>C (p.Lys913Thr)	rs1060503649	0.00001
NM_177438.3(DICER1):c.3229G>A (p.Asp1077Asn)	rs373412959	0.00001
NM_177438.3(DICER1):c.3496G>A (p.Val1166Ile)	rs368588781	0.00001
NM_177438.3(DICER1):c.3752C>T (p.Thr1251Ile)	rs2139960558	0.00001
NM_177438.3(DICER1):c.493T>C (p.Ser165Pro)	rs894664317	0.00001
NM_177438.3(DICER1):c.5762A>G (p.Asn1921Ser)	rs764747360	0.00001
NM_177438.3(DICER1):c.698A>G (p.Asn233Ser)	rs1465088683	0.00001
NM_177438.3(DICER1):c.920G>A (p.Arg307His)	rs149718671	0.00001
NM_177438.3(DICER1):c.956A>T (p.Asp319Val)	rs776738577	0.00001
NM_177438.3(DICER1):c.1257T>G (p.Asp419Glu)	rs2543174828
NM_177438.3(DICER1):c.2823G>T (p.Gln941His)	rs1891411377
NM_177438.3(DICER1):c.3631G>C (p.Val1211Leu)	rs764470378
NM_177438.3(DICER1):c.3635A>C (p.Gln1212Pro)	rs763415569
NM_177438.3(DICER1):c.3785C>G (p.Pro1262Arg)	rs1595364864
NM_177438.3(DICER1):c.4178_4180dup (p.Asn1393dup)	rs878855263
NM_177438.3(DICER1):c.4216T>G (p.Cys1406Gly)	rs1356179383
NM_177438.3(DICER1):c.4226C>T (p.Ala1409Val)	rs776416084
NM_177438.3(DICER1):c.4838A>T (p.Gln1613Leu)	rs775024028
NM_177438.3(DICER1):c.5013G>T (p.Lys1671Asn)	rs751819396
NM_177438.3(DICER1):c.5761A>G (p.Asn1921Asp)	rs775077210
NM_177438.3(DICER1):c.712A>G (p.Thr238Ala)	rs760627991

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