ClinVar Miner

List of variants reported as benign for childhood malignant neoplasm

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_177438.3(DICER1):c.4206+9G>T rs1778057 0.25695
NM_177438.3(DICER1):c.4680G>A (p.Ala1560=) rs61729797 0.03654
NM_177438.3(DICER1):c.3033G>A (p.Ala1011=) rs8019857 0.03643
NM_177438.3(DICER1):c.2997T>G (p.Leu999=) rs12018992 0.01764
NM_177438.3(DICER1):c.3198T>C (p.Thr1066=) rs114964211 0.01414
NM_177438.3(DICER1):c.1935G>A (p.Pro645=) rs61751177 0.00958
NM_177438.3(DICER1):c.1887G>A (p.Thr629=) rs141651702 0.00806
NM_177438.3(DICER1):c.2370G>A (p.Arg790=) rs112712209 0.00777
NM_177438.3(DICER1):c.5095+13C>T rs116247322 0.00577
NM_177438.3(DICER1):c.5241G>A (p.Ser1747=) rs114861074 0.00539
NM_177438.3(DICER1):c.1377-4T>G rs192490028 0.00240
NM_177438.3(DICER1):c.3972G>A (p.Lys1324=) rs45562437 0.00174
NM_177438.3(DICER1):c.20A>G (p.Gln7Arg) rs117358479 0.00165
NM_177438.3(DICER1):c.2614G>A (p.Ala872Thr) rs149242330 0.00074
NM_177438.3(DICER1):c.924C>T (p.Ala308=) rs142397473 0.00070
NM_177438.3(DICER1):c.4407T>C (p.Leu1469=) rs540502223 0.00002
NM_177438.3(DICER1):c.*1448dup rs35463377
NM_177438.3(DICER1):c.*1716TG[1] rs35500699
NM_177438.3(DICER1):c.*2379dup rs140355178
NM_177438.3(DICER1):c.4206+7_4206+8dup rs1555368535

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