ClinVar Miner

List of variants in gene IARS2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NC_000001.11:g.220093910del rs57957113 0.46897
NM_018060.4(IARS2):c.950+214A>G rs2789789 0.46839
NM_018060.4(IARS2):c.551-93G>A rs2789788 0.46818
NM_018060.4(IARS2):c.2415-200G>A rs10442693 0.39786
NM_018060.4(IARS2):c.391-268T>G rs2289190 0.26063
NM_018060.4(IARS2):c.2414+222G>A rs3738337 0.25164
NC_000001.11:g.220093908A>T rs58943245 0.16032
NM_018060.4(IARS2):c.*46A>G rs11095 0.14776
NM_018060.4(IARS2):c.2896+115A>G rs3738336 0.14546
NM_018060.4(IARS2):c.950+185C>T rs17563518 0.14442
NM_018060.4(IARS2):c.1946+258G>T rs201023394 0.14440
NM_018060.4(IARS2):c.551-297C>G rs60531981 0.14074
NM_018060.4(IARS2):c.2897-294A>G rs59914129 0.13248
NM_018060.4(IARS2):c.1480-195C>T rs73096599 0.12604
NC_000001.11:g.220093910_220093912del rs570325367 0.09853
NM_018060.4(IARS2):c.2414+84A>G rs141385141 0.09093
NM_018060.4(IARS2):c.2896+306T>G rs11806086 0.08585
NM_018060.4(IARS2):c.2896+12A>G rs75519000 0.07588
NM_018060.4(IARS2):c.268-7A>T rs78836180 0.07149
NM_018060.4(IARS2):c.390+232C>T rs78887187 0.06873
NM_018060.4(IARS2):c.1480-306C>T rs75886035 0.06854
NC_000001.11:g.220093912del rs1193637553 0.06236
NM_018060.4(IARS2):c.1838-68A>G rs35775533 0.05821
NM_018060.4(IARS2):c.551-301G>A rs142081039 0.05347
NM_018060.4(IARS2):c.1744-57T>C rs2289191 0.05337
NM_018060.4(IARS2):c.2049+94A>C rs74902866 0.05335
NM_018060.4(IARS2):c.2752-329T>C rs75657857 0.05219
NM_018060.4(IARS2):c.1066+191T>G rs58256586 0.05084
NM_018060.4(IARS2):c.1726A>G (p.Lys576Glu) rs78770848 0.03301
NM_018060.4(IARS2):c.2415-169C>T rs146345863 0.01905
NM_018060.4(IARS2):c.1564A>G (p.Ile522Val) rs11800305 0.01131
NM_018060.4(IARS2):c.942T>C (p.Pro314=) rs148564492 0.00307
NM_018060.4(IARS2):c.1164G>A (p.Thr388=) rs143373097 0.00282
NM_018060.4(IARS2):c.700-11G>C rs182226161 0.00276
NC_000001.11:g.220093907_220093909del rs374211356
NC_000001.11:g.220093908_220093909del rs374211356
NC_000001.11:g.220093908_220093911del rs1450097145
NC_000001.11:g.220093909_220093911del rs774844700
NC_000001.11:g.220093909del rs374211356
NM_018060.4(IARS2):c.1328-5del rs199649609
NM_018060.4(IARS2):c.1328-5dup rs199649609
NM_018060.4(IARS2):c.1946+275del rs57598038
NM_018060.4(IARS2):c.1946+287G>T rs45454400
NM_018060.4(IARS2):c.1947-351G>C rs73098527
NM_018060.4(IARS2):c.551-3del rs574253271

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