ClinVar Miner

List of variants in gene CALR3 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_145046.5(CALR3):c.919-183A>G rs8111530 0.88876
NM_145046.5(CALR3):c.91+84C>G rs3810200 0.84239
NM_145046.5(CALR3):c.92-79C>G rs3810199 0.83542
NM_145046.5(CALR3):c.918+58T>C rs75847259 0.68538
NM_145046.5(CALR3):c.1012-86A>C rs12459647 0.66972
NM_145046.5(CALR3):c.787-23C>T rs8100755 0.66944
NC_000019.10:g.16478939T>C rs8103521 0.66900
NM_145046.5(CALR3):c.919-178C>T rs10414751 0.66893
NM_145046.5(CALR3):c.493-41T>C rs10413787 0.66811
NM_145046.5(CALR3):c.1012-175C>T rs2216669 0.66805
NM_145046.5(CALR3):c.1011+251T>C rs10410819 0.66640
NM_145046.5(CALR3):c.381G>A (p.Gln127=) rs3810198 0.66498
NM_145046.5(CALR3):c.493-53G>A rs7252242 0.66150
NM_145046.5(CALR3):c.972C>T (p.Tyr324=) rs9305079 0.65389
NM_145046.5(CALR3):c.1011+189C>T rs10413805 0.62960
NM_145046.5(CALR3):c.397+24A>G rs3810196 0.62703
NM_145046.5(CALR3):c.918+249G>A rs8112401 0.62517
NM_145046.5(CALR3):c.679-186T>C rs10405924 0.16943
NM_145046.5(CALR3):c.702C>T (p.Asp234=) rs10403020 0.16282
NM_145046.5(CALR3):c.397+10C>T rs3810197 0.12536
NM_145046.5(CALR3):c.194-30T>A rs79268770 0.04679
NC_000019.10:g.16496310C>T rs11667136 0.04140
NM_145046.5(CALR3):c.194-90T>C rs77302641 0.03651
NC_000019.10:g.16478996A>G rs118051449 0.03240
NM_145046.5(CALR3):c.1011+187G>A rs143709489 0.02844
NM_145046.5(CALR3):c.820G>A (p.Val274Ile) rs12459238 0.02701
NM_145046.5(CALR3):c.861G>A (p.Thr287=) rs118131979 0.01174
NM_145046.5(CALR3):c.1012-167dup rs67714289
NM_145046.5(CALR3):c.193+172_193+173dup rs57877938
NM_145046.5(CALR3):c.193+172dup rs57877938
NM_145046.5(CALR3):c.193+190_193+192del rs57877938
NM_145046.5(CALR3):c.193+191_193+192del rs57877938
NM_145046.5(CALR3):c.194-194del rs78242115
NM_145046.5(CALR3):c.493-64del rs71334622
NM_145046.5(CALR3):c.493-64dup rs71334622
NM_145046.5(CALR3):c.679-184G>T rs10405116
NM_145046.5(CALR3):c.918+321G>T rs12982918
NM_145046.5(CALR3):c.918+47TTGTT[4] rs71178697

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