ClinVar Miner

List of variants in gene DNMT3B reported as benign for autosomal recessive disease

Included ClinVar conditions (1196):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_006892.4(DNMT3B):c.2302-212T>C rs4911263 0.79668
NM_006892.4(DNMT3B):c.*827A>G rs2424932 0.71093
NM_006892.4(DNMT3B):c.1906-5T>C rs2424928 0.58051
NM_006892.4(DNMT3B):c.1760-5C>G rs1997797 0.55509
NC_000020.11:g.32762102T>C rs6087990 0.52775
NM_006892.4(DNMT3B):c.307-49C>T rs2424913 0.52532
NM_006892.4(DNMT3B):c.143-22del rs3835238 0.45870
NM_006892.4(DNMT3B):c.1252+13T>G rs910085 0.42898
NM_006892.4(DNMT3B):c.*443C>T rs6058896 0.07771
NM_006892.4(DNMT3B):c.1881C>T (p.Asp627=) rs17123657 0.05837
NM_006892.4(DNMT3B):c.1760-17C>T rs76661393 0.02476
NM_006892.4(DNMT3B):c.1878C>T (p.Asn626=) rs17123655 0.02475
NM_006892.4(DNMT3B):c.1996+6C>T rs77355896 0.01863
NM_006892.4(DNMT3B):c.1413C>T (p.Asp471=) rs6119965 0.01256
NM_006892.4(DNMT3B):c.1150G>A (p.Ala384Thr) rs150682895 0.00967
NM_006892.4(DNMT3B):c.*75C>G rs6119971 0.00868
NM_006892.4(DNMT3B):c.*895T>C rs116329759 0.00684
NM_006892.4(DNMT3B):c.1996+9C>T rs143448185 0.00128
NM_006892.4(DNMT3B):c.922-8C>T rs200508870 0.00076
NM_006892.4(DNMT3B):c.204+13C>T rs560602182 0.00054
NM_006892.4(DNMT3B):c.2445C>T (p.Tyr815=) rs560320736 0.00027
NM_006892.4(DNMT3B):c.42C>T (p.Ala14=) rs730823 0.00027
NM_006892.4(DNMT3B):c.1923A>G (p.Pro641=) rs555058105 0.00025
NM_006892.4(DNMT3B):c.1211A>G (p.Tyr404Cys) rs143462810 0.00023
NM_006892.4(DNMT3B):c.307-15C>G rs150718732 0.00018
NM_006892.4(DNMT3B):c.1126+15T>C rs150368389 0.00016
NM_006892.4(DNMT3B):c.2055G>A (p.Lys685=) rs144497819 0.00010
NM_006892.4(DNMT3B):c.336C>T (p.Ser112=) rs199763590 0.00008
NM_006892.4(DNMT3B):c.1215C>T (p.Asn405=) rs183617300 0.00004
NM_006892.4(DNMT3B):c.*1318del rs398088406
NM_006892.4(DNMT3B):c.1359G>A (p.Gly453=) rs35216603
NM_006892.4(DNMT3B):c.1760-5del
NM_006892.4(DNMT3B):c.1760-8C>G rs2424926
NM_006892.4(DNMT3B):c.1760-8C>T rs2424926
NM_006892.4(DNMT3B):c.1920C>T (p.Gly640=) rs532347792
NM_006892.4(DNMT3B):c.349C>T (p.His117Tyr) rs559899499

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