ClinVar Miner

List of variants in gene RUNX1 reported as benign for not provided

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001754.5(RUNX1):c.614-34C>T rs11702841 0.99999
NM_001754.5(RUNX1):c.805+12836A>G rs2018329 0.81294
NM_001754.5(RUNX1):c.58+103A>G rs8133634 0.59069
NM_001754.5(RUNX1):c.968-134A>G rs11700756 0.53695
NM_001754.5(RUNX1):c.*27C>A rs13051066 0.36204
NM_001754.5(RUNX1):c.352-184A>T rs2298354 0.25699
NM_001754.5(RUNX1):c.508+259C>T rs2298351 0.23830
NM_001754.5(RUNX1):c.508+232A>G rs2298352 0.23437
NM_001754.5(RUNX1):c.351+301A>G rs8126699 0.17527
NM_001754.5(RUNX1):c.1389C>G (p.Pro463=) rs61750222 0.04709
NC_000021.9:g.34787766A>G rs79178911 0.04515
NM_001754.5(RUNX1):c.805+186C>T rs55789220 0.03584
NM_001754.5(RUNX1):c.*70T>C rs150481777 0.03364
NM_001754.5(RUNX1):c.*4032T>C rs78335539 0.02935
NM_001754.5(RUNX1):c.968-269G>A rs73362834 0.02871
NM_001754.5(RUNX1):c.*88G>T rs539980908 0.02200
NM_001754.5(RUNX1):c.352-292T>C rs111271072 0.01560
NM_001754.5(RUNX1):c.167T>C (p.Leu56Ser) rs111527738 0.01206
NM_001754.5(RUNX1):c.144C>T (p.Ser48=) rs147889692 0.00344
GRCh37/hg19 21q22.12(chr21:36255821-36262143)x1
GRCh37/hg19 21q22.12(chr21:36261125-36262031)x1
GRCh37/hg19 21q22.12(chr21:36261125-36262143)x1
GRCh37/hg19 21q22.12(chr21:36261631-36464906)x3
NC_000021.9:g.35049406del rs57713477
NM_001754.5(RUNX1):c.*4140C>T rs141693054
NM_001754.5(RUNX1):c.352-141_352-137del rs56243517
NM_001754.5(RUNX1):c.509-281G>T rs2248720
NM_001754.5(RUNX1):c.98-155dup rs3833348

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