ClinVar Miner

List of variants in gene GRN reported by Athena Diagnostics Inc

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
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.1544G>C (p.Gly515Ala) rs25647 0.00781
NM_002087.4(GRN):c.264+7G>A rs60100877 0.00548
NM_002087.4(GRN):c.42G>A (p.Leu14=) rs111435385 0.00533
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.1227G>A (p.Thr409=) rs140298583 0.00326
NM_002087.4(GRN):c.-38T>C rs530686556 0.00325
NM_002087.4(GRN):c.1298G>A (p.Arg433Gln) rs114248177 0.00247
NM_002087.4(GRN):c.970G>A (p.Ala324Thr) rs63750541 0.00112
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_002087.4(GRN):c.253C>G (p.Pro85Ala) rs143560849 0.00058
NM_002087.3(GRN):c.-45C>G rs563336550 0.00057
NM_002087.4(GRN):c.393C>G (p.Phe131Leu) rs149180605 0.00052
NM_002087.4(GRN):c.903G>A (p.Ser301=) rs63750142 0.00044
NM_002087.3(GRN):c.-56T>G rs909307115 0.00032
NM_002087.4(GRN):c.1253G>A (p.Arg418Gln) rs63751100 0.00022
NM_002087.3(GRN):c.-203G>C rs555738837 0.00010
NM_002087.3(GRN):c.-100A>G rs956983853 0.00008
NM_002087.4(GRN):c.1742A>T (p.Asp581Val) rs768223928 0.00007
NM_002087.4(GRN):c.1641C>T (p.Arg547=) rs149658268 0.00006
NM_002087.4(GRN):c.803C>T (p.Thr268Met) rs202006119 0.00005
NM_002087.4(GRN):c.1112G>C (p.Ser371Thr) rs149023078 0.00003
NM_002087.4(GRN):c.421G>A (p.Val141Ile) rs63749853 0.00002
NM_002087.4(GRN):c.836-3C>T rs771907059 0.00002
NM_002087.4(GRN):c.1010_1011del (p.Gln337fs) rs1598364961 0.00001
NM_002087.4(GRN):c.1448C>T (p.Pro483Leu) rs774128685 0.00001
NM_002087.4(GRN):c.1477C>T (p.Arg493Ter) rs63751294 0.00001
NM_002087.4(GRN):c.928A>C (p.Thr310Pro) rs969767392 0.00001
NM_002087.4(GRN):c.102del (p.Gly35fs) rs63751073
NM_002087.4(GRN):c.1072C>T (p.Gln358Ter) rs1555611293
NM_002087.4(GRN):c.1073_1074dup (p.Ala359fs) rs1567887567
NM_002087.4(GRN):c.1252C>T (p.Arg418Ter) rs63751180
NM_002087.4(GRN):c.1414-2A>G rs1555611412
NM_002087.4(GRN):c.1420_1421del (p.Cys474fs) rs2048384991
NM_002087.4(GRN):c.1465_1469dup (p.Lys491fs) rs1555611439
NM_002087.4(GRN):c.26C>A (p.Ala9Asp) rs63751243
NM_002087.4(GRN):c.328C>T (p.Arg110Ter) rs63750411
NM_002087.4(GRN):c.388_391del (p.Gln130fs) rs63749801
NM_002087.4(GRN):c.592_593del (p.Arg198fs) rs1555611136
NM_002087.4(GRN):c.599-1G>A rs1555611154
NM_002087.4(GRN):c.675_676del (p.Ser226fs) rs63751085
NM_002087.4(GRN):c.6G>A (p.Trp2Ter) rs1555610855
NM_002087.4(GRN):c.768_769dup (p.Gln257fs) rs1567887004
NM_002087.4(GRN):c.813_816del (p.Thr272fs) rs63749877
NM_002087.4(GRN):c.837G>A (p.Val279=)
NM_002087.4(GRN):c.898C>T (p.Gln300Ter) rs1555611253
NM_002087.4(GRN):c.911G>A (p.Trp304Ter) rs63751177
NM_002087.4(GRN):c.99C>T (p.Asp33=) rs63750742

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