ClinVar Miner

List of variants in gene SARM1, SLC46A1 studied for anemia (disease)

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP
NM_080669.5(SLC46A1):c.*1006A>C rs886052749
NM_080669.5(SLC46A1):c.*1062G>A rs535633260
NM_080669.5(SLC46A1):c.*1076G>A rs151184490
NM_080669.5(SLC46A1):c.*1094A>G rs782533706
NM_080669.5(SLC46A1):c.*11C>T rs782615925
NM_080669.5(SLC46A1):c.*1220A>G rs886052748
NM_080669.5(SLC46A1):c.*1243A>G rs41297909
NM_080669.5(SLC46A1):c.*129C>T rs886052752
NM_080669.5(SLC46A1):c.*1332G>A rs146041886
NM_080669.5(SLC46A1):c.*1392C>A rs141940033
NM_080669.5(SLC46A1):c.*1407C>T rs2239908
NM_080669.5(SLC46A1):c.*1627T>A rs886052747
NM_080669.5(SLC46A1):c.*1648G>A rs114008979
NM_080669.5(SLC46A1):c.*1649A>G rs779490495
NM_080669.5(SLC46A1):c.*1774A>G rs2239909
NM_080669.5(SLC46A1):c.*1795C>T rs200529579
NM_080669.5(SLC46A1):c.*1831C>A rs41297915
NM_080669.5(SLC46A1):c.*1981C>G rs41297919
NM_080669.5(SLC46A1):c.*2123G>C rs7225850
NM_080669.5(SLC46A1):c.*2248T>C rs8082600
NM_080669.5(SLC46A1):c.*2273A>G rs542078425
NM_080669.5(SLC46A1):c.*2401G>A rs555975005
NM_080669.5(SLC46A1):c.*2493A>G rs886052746
NM_080669.5(SLC46A1):c.*2513G>C rs576823032
NM_080669.5(SLC46A1):c.*2558C>T rs750056802
NM_080669.5(SLC46A1):c.*2636C>A rs782382359
NM_080669.5(SLC46A1):c.*2661G>C rs886052745
NM_080669.5(SLC46A1):c.*277A>G rs886052751
NM_080669.5(SLC46A1):c.*2808G>C rs886052744
NM_080669.5(SLC46A1):c.*2843G>A rs118138669
NM_080669.5(SLC46A1):c.*2853G>A rs739439
NM_080669.5(SLC46A1):c.*2968C>T rs12453383
NM_080669.5(SLC46A1):c.*3009G= rs2239910
NM_080669.5(SLC46A1):c.*3009G>A rs2239910
NM_080669.5(SLC46A1):c.*3062C>A rs2239911
NM_080669.5(SLC46A1):c.*3135A>G rs762983414
NM_080669.5(SLC46A1):c.*3203A>G rs886052743
NM_080669.5(SLC46A1):c.*3266G>A rs73273104
NM_080669.5(SLC46A1):c.*3302A>G rs886052742
NM_080669.5(SLC46A1):c.*3389G>A rs146812537
NM_080669.5(SLC46A1):c.*3402A>G rs781986662
NM_080669.5(SLC46A1):c.*3603C>T rs782370729
NM_080669.5(SLC46A1):c.*3661T>C rs782774927
NM_080669.5(SLC46A1):c.*3677C>G rs886052741
NM_080669.5(SLC46A1):c.*3785T>C rs117451747
NM_080669.5(SLC46A1):c.*3789C>A rs886052740
NM_080669.5(SLC46A1):c.*3913A>T rs886052739
NM_080669.5(SLC46A1):c.*3947G>A rs8081240
NM_080669.5(SLC46A1):c.*3959C>G rs886052738
NM_080669.5(SLC46A1):c.*4030C>T rs8079943
NM_080669.5(SLC46A1):c.*4316C>G rs117397871
NM_080669.5(SLC46A1):c.*4320A>G rs528235797
NM_080669.5(SLC46A1):c.*4323C>G rs561043242
NM_080669.5(SLC46A1):c.*4634_*4635dupTT rs34879232
NM_080669.5(SLC46A1):c.*4635dupT rs34879232
NM_080669.5(SLC46A1):c.*4636C>T rs886052737
NM_080669.5(SLC46A1):c.*4661G>A rs575926704
NM_080669.5(SLC46A1):c.*4729delC rs559270240
NM_080669.5(SLC46A1):c.*4742A>G rs886052736
NM_080669.5(SLC46A1):c.*4780C>T rs1128161
NM_080669.5(SLC46A1):c.*4884G>T rs1128162
NM_080669.5(SLC46A1):c.*4G>T rs886052753
NM_080669.5(SLC46A1):c.*60G>T rs41297121
NM_080669.5(SLC46A1):c.*692A>T rs112801276
NM_080669.5(SLC46A1):c.*729G>A rs41297903
NM_080669.5(SLC46A1):c.*785T>G rs886052750
NM_080669.5(SLC46A1):c.*835A>G rs181698246
NM_080669.5(SLC46A1):c.*90G>A rs782079474
NM_080669.5(SLC46A1):c.*928A>G rs2239907
NM_080669.5(SLC46A1):c.1082-1G>A rs80338775
NM_080669.5(SLC46A1):c.1126C>T (p.Arg376Trp) rs80338773
NM_080669.5(SLC46A1):c.1127G>A (p.Arg376Gln) rs281875211
NM_080669.5(SLC46A1):c.1274C>G (p.Pro425Arg) rs80338774
NM_080669.5(SLC46A1):c.1367C>T (p.Pro456Leu) rs886052754

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