List of variants in gene combination DNMT3B, LOC130065670 reported as uncertain significance for autosomal recessive disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_006892.4(DNMT3B):c.-303G>A	rs909287301	0.00019
NM_006892.4(DNMT3B):c.-212C>T	rs749909518	0.00008
NM_006892.4(DNMT3B):c.-163A>C	rs545638472	0.00007
NM_006892.4(DNMT3B):c.-105C>T	rs767131541	0.00003
NM_006892.4(DNMT3B):c.-267C>A	rs751398063	0.00002
NM_006892.4(DNMT3B):c.-62C>G	rs886056612	0.00002
NM_006892.4(DNMT3B):c.-224C>A	rs886056611	0.00001
NM_006892.4(DNMT3B):c.-21C>T	rs542835821
NM_006892.4(DNMT3B):c.-234G>C	rs756914098
NM_006892.4(DNMT3B):c.-264C>T	rs1365103113

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