ClinVar Miner

List of intergenic variants reported as other for colorectal cancer

Included ClinVar conditions (91):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP gnomAD frequency
NC_000005.10:g.112850367C>A rs481789 0.66441
NC_000005.10:g.112849754A>G rs565603 0.63961
NC_000005.10:g.112849696A>C rs565453 0.63945
NC_000005.10:g.112849794A>G rs497844 0.63937
NM_000038.5(APC):c.*2409A>T rs433429 0.62297
NM_000038.5(APC):c.*2556G>A rs386830 0.62272
NC_000005.10:g.112846994A>G rs448162 0.49508
NC_000005.10:g.112848793T>C rs2545155 0.42089
NC_000005.10:g.112847460A>G rs2546112 0.41030
NC_000005.10:g.112849816A>C rs566419 0.40988
NC_000005.10:g.112849377A>T rs7729562 0.11367
NC_000005.10:g.112848450G>T rs79226141 0.02861
NC_000005.10:g.112849375T>A rs78959697 0.00013
NC_000005.10:g.112851087G>T rs78153755 0.00002
NC_000005.10:g.112847807G>T rs74849978 0.00001
NC_000005.10:g.112849133A>G rs79781960 0.00001
NC_000005.10:g.112849376T>A rs76990810 0.00001
NC_000005.10:g.112851086G>T rs79636346 0.00001
NC_000005.10:g.112851098T>C rs74365481 0.00001
NC_000005.10:g.112846779C>A rs76630706
NC_000005.10:g.112847402A>C rs74947963
NC_000005.10:g.112847796G>T rs80136756
NC_000005.10:g.112847814T>C rs74861083
NC_000005.10:g.112848559A>C rs77718736
NC_000005.10:g.112848623A>G rs77550653
NC_000005.10:g.112848647C>T rs75078014
NC_000005.10:g.112848715G>A rs78319369
NC_000005.10:g.112848716A>G rs79221286
NC_000005.10:g.112848914T>C rs77639923
NC_000005.10:g.112849086T>G rs75838239
NC_000005.10:g.112849089C>G rs76217399
NC_000005.10:g.112849092A>C rs75316587
NC_000005.10:g.112849163G>C rs76832814
NC_000005.10:g.112849265A>C rs74784138
NC_000005.10:g.112849302A>G rs75665127
NC_000005.10:g.112849304C>G rs76754349
NC_000005.10:g.112849374A>T rs80318527
NC_000005.10:g.112849397G>A rs75121906
NC_000005.10:g.112849398A>G rs76001065
NC_000005.10:g.112849707G>T rs78413161
NC_000005.10:g.112849722C>A rs75765930
NC_000005.10:g.112849729C>A rs75828475
NC_000005.10:g.112849895G>T rs78424514
NC_000005.10:g.112850623A>C rs76962693
NC_000005.10:g.112850623A>G rs76962693
NC_000005.10:g.112850624C>A rs74737621
NC_000005.10:g.112850816T>A rs77990042
NC_000005.10:g.112850818C>A rs76105561
NC_000005.10:g.112850819A>C rs76608198
NC_000005.10:g.112850820C>A rs74713622
NC_000005.10:g.112850821A>C rs75756946
NC_000005.10:g.112850822G>A rs76350436
NC_000005.10:g.112850823A>T rs75078263
NC_000005.10:g.112850824C>G rs79675475
NC_000005.10:g.112850826A>G rs77168313
NC_000005.10:g.112850827A>T rs78513107
NC_000005.10:g.112850828T>G rs78756699
NC_000005.10:g.112850829T>C rs79660756
NC_000005.10:g.112850830C>A rs78075831
NC_000005.10:g.112850831A>G rs78988154
NC_000005.10:g.112850832T>C rs77687441
NC_000005.10:g.112850833C>A rs75473948
NC_000005.10:g.112850835G>A rs79881752
NC_000005.10:g.112850836T>C rs74419699
NC_000005.10:g.112850837A>C rs79021693
NC_000005.10:g.112851075A>C rs76530936
NC_000005.10:g.112851076G>T rs73220029
NC_000005.10:g.112851077T>C rs75395853
NC_000005.10:g.112851079G>T rs76458454
NC_000005.10:g.112851080A>T rs78260346
NC_000005.10:g.112851081G>T rs76292134
NC_000005.10:g.112851082A>T rs80071664
NC_000005.10:g.112851083C>G rs74904155
NC_000005.10:g.112851085G>T rs78555612
NC_000005.10:g.112851089T>G rs78782405
NC_000005.10:g.112851090T>C rs77267811
NC_000005.10:g.112851092A>C rs78799443
NC_000005.10:g.112851093C>T rs76660336
NC_000005.10:g.112851094C>G rs77512690
NC_000005.10:g.112851096T>G rs74882763
NC_000005.10:g.112851097T>C rs75931773
NC_000005.10:g.112851099T>A rs75491288
NC_000005.10:g.112851100G>C rs80162849
NC_000005.10:g.112851101G>A rs74730119
NC_000005.10:g.112851102T>A rs79275719
NC_000005.10:g.112851103C>A rs77018630
NM_000038.5(APC):c.*2292A>T rs77771787
NM_000038.5(APC):c.*2293A>T rs78516426
NM_000038.5(APC):c.*2294C>G rs77843403
NM_000038.5(APC):c.*2296T>G rs75293893
NM_000038.5(APC):c.*2542T>G rs77333076
NM_000038.5(APC):c.*2543T>G rs76955943
NM_000038.5(APC):c.*2546G>A rs76130955
NM_000038.5(APC):c.*2590A>G rs78002373

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