ClinVar Miner

List of variants in gene GRN reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_002087.4(GRN):c.*78C>T rs5848 0.41298
NM_002087.4(GRN):c.835+7G>A rs72824736 0.04753
NM_002087.4(GRN):c.384T>C (p.Asp128=) rs25646 0.02616
NM_002087.4(GRN):c.55C>T (p.Arg19Trp) rs63750723 0.01303
NM_002087.4(GRN):c.*280G>A rs116547342 0.01005
NM_002087.4(GRN):c.1544G>C (p.Gly515Ala) rs25647 0.00781
NM_002087.3(GRN):c.-72G>T rs76783532 0.00635
NM_002087.4(GRN):c.264+7G>A rs60100877 0.00548
NM_002087.4(GRN):c.1297C>T (p.Arg433Trp) rs63750412 0.00523
NM_002087.4(GRN):c.545C>T (p.Thr182Met) rs63750479 0.00356
NM_002087.4(GRN):c.546G>A (p.Thr182=) rs138473783 0.00335
NM_002087.4(GRN):c.-38T>C rs530686556 0.00325
NM_002087.4(GRN):c.970G>A (p.Ala324Thr) rs63750541 0.00112
NM_002087.4(GRN):c.*246A>G rs552375884 0.00096
NM_002087.4(GRN):c.228C>T (p.Thr76=) rs144736470 0.00086
NM_002087.4(GRN):c.359C>A (p.Ser120Tyr) rs63750043 0.00076
NM_002087.3(GRN):c.-45C>G rs563336550 0.00057
NM_002087.4(GRN):c.903G>A (p.Ser301=) rs63750142 0.00044
NM_002087.4(GRN):c.1253G>A (p.Arg418Gln) rs63751100 0.00022
NM_002087.4(GRN):c.-22C>T rs572309824 0.00009
NM_002087.4(GRN):c.1647C>T (p.Gly549=) rs745391227 0.00009
NM_002087.4(GRN):c.497C>T (p.Pro166Leu) rs368705304 0.00009
NM_002087.3(GRN):c.-100A>G rs956983853 0.00008
NM_002087.4(GRN):c.1341C>T (p.His447=) rs63750775 0.00008
NM_002087.4(GRN):c.626C>T (p.Pro209Leu) rs368995988 0.00008
NM_002087.4(GRN):c.1641C>T (p.Arg547=) rs149658268 0.00006
NM_002087.4(GRN):c.268G>A (p.Val90Met) rs200019356 0.00006
NM_002087.4(GRN):c.933+15C>T rs1306228988 0.00005
NM_002087.4(GRN):c.57G>T (p.Arg19=) rs1426790644 0.00003
NM_002087.4(GRN):c.1373C>T (p.Pro458Leu) rs63750537 0.00002
NM_002087.4(GRN):c.139-3T>C rs371119011 0.00002
NM_002087.4(GRN):c.835+14G>C rs753286440 0.00002
NM_002087.3(GRN):c.-173C>T rs886053004 0.00001
NM_002087.3(GRN):c.-179G>C rs886053003 0.00001
NM_002087.4(GRN):c.*12G>T rs775440171 0.00001
NM_002087.4(GRN):c.*273C>T rs971394484 0.00001
NM_002087.4(GRN):c.*30G>A rs374114836 0.00001
NM_002087.4(GRN):c.1019A>T (p.His340Leu) rs775196555 0.00001
NM_002087.4(GRN):c.1180-8C>T rs774308165 0.00001
NM_002087.4(GRN):c.1357G>A (p.Gly453Arg) rs751072702 0.00001
NM_002087.4(GRN):c.1521C>T (p.Phe507=) rs140070738 0.00001
NM_002087.3(GRN):c.-212G>A rs886053002
NM_002087.4(GRN):c.-8+3A>C rs63751020
NM_002087.4(GRN):c.100C>G (p.Pro34Ala) rs748147151
NM_002087.4(GRN):c.1087_1088del (p.Asp363fs) rs1567887576
NM_002087.4(GRN):c.1120TCC[1] (p.Ser375del) rs754862784
NM_002087.4(GRN):c.1179+6T>C rs765761482
NM_002087.4(GRN):c.1180-8C>A rs774308165
NM_002087.4(GRN):c.1468G>A (p.Val490Met) rs886053006
NM_002087.4(GRN):c.1518C>T (p.Thr506=) rs768852944
NM_002087.4(GRN):c.1548G>T (p.Val516=) rs1044281109
NM_002087.4(GRN):c.1560G>T (p.Glu520Asp) rs1242287545
NM_002087.4(GRN):c.393C>T (p.Phe131=) rs149180605
NM_002087.4(GRN):c.99C>A (p.Asp33Glu) rs63750742
NM_002087.4(GRN):c.99C>T (p.Asp33=) rs63750742

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