ClinVar Miner

List of variants in gene GGCX reported as uncertain significance for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 128
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HGVS dbSNP gnomAD frequency
NM_000821.7(GGCX):c.*107T>G rs78909830 0.04352
NM_000821.7(GGCX):c.*3770T>C rs141040739 0.00627
NM_000821.7(GGCX):c.*108G>T rs886056378 0.00434
NM_000821.7(GGCX):c.*4413T>C rs144074011 0.00426
NM_000821.7(GGCX):c.*338T>C rs539761806 0.00222
NM_000821.7(GGCX):c.*1245G>C rs190566964 0.00175
NM_000821.7(GGCX):c.*4562G>A rs113066451 0.00099
NM_000821.7(GGCX):c.1743G>A (p.Leu581=) rs56165933 0.00096
NM_000821.7(GGCX):c.*3192C>T rs150878929 0.00091
NM_000821.7(GGCX):c.159C>A (p.Thr53=) rs61733104 0.00090
NM_000821.7(GGCX):c.*1725C>A rs184184818 0.00085
NM_000821.7(GGCX):c.*3647A>G rs541759232 0.00075
NM_000821.7(GGCX):c.789C>T (p.Asp263=) rs146085955 0.00071
NM_000821.7(GGCX):c.529A>G (p.Asn177Asp) rs149039591 0.00070
NM_000821.7(GGCX):c.*2408T>C rs556052128 0.00054
NM_000821.7(GGCX):c.1906C>A (p.Pro636Thr) rs61733105 0.00054
NM_000821.7(GGCX):c.*2490T>C rs574322048 0.00052
NM_000821.7(GGCX):c.*1367C>A rs559519177 0.00051
NM_000821.7(GGCX):c.*454C>T rs578230076 0.00047
NM_000821.7(GGCX):c.*4242C>G rs754152731 0.00044
NM_000821.7(GGCX):c.*1698A>G rs143548117 0.00042
NM_000821.7(GGCX):c.*3269A>G rs563109158 0.00041
NM_000821.7(GGCX):c.*469C>T rs557756406 0.00041
NM_000821.7(GGCX):c.*270T>G rs886056377 0.00034
NM_000821.7(GGCX):c.*598C>T rs553605433 0.00034
NM_000821.7(GGCX):c.1355G>C (p.Ser452Thr) rs144429522 0.00031
NM_000821.7(GGCX):c.1107C>T (p.Leu369=) rs145056129 0.00029
NM_000821.7(GGCX):c.*106T>G rs530539627 0.00028
NM_000821.7(GGCX):c.24G>A (p.Ala8=) rs371622780 0.00026
NM_000821.7(GGCX):c.849G>C (p.Val283=) rs149603998 0.00025
NM_000821.7(GGCX):c.*3584C>T rs748992023 0.00024
NM_000821.7(GGCX):c.*2060T>C rs886056369 0.00021
NM_000821.7(GGCX):c.*2284C>G rs572084939 0.00019
NM_000821.7(GGCX):c.*2285T>A rs553827130 0.00019
NM_000821.7(GGCX):c.*3921G>A rs886056360 0.00019
NM_000821.7(GGCX):c.540-8C>T rs374625413 0.00018
NM_000821.7(GGCX):c.*2925G>C rs188039599 0.00016
NM_000821.7(GGCX):c.*3704G>A rs375566923 0.00016
NM_000821.7(GGCX):c.*3930T>C rs1046049435 0.00016
NM_000821.7(GGCX):c.*4195T>G rs536985458 0.00015
NM_000821.7(GGCX):c.2081G>A (p.Arg694His) rs140098905 0.00014
NM_000821.7(GGCX):c.*470G>A rs746348970 0.00013
NM_000821.7(GGCX):c.2254G>C (p.Asp752His) rs201917261 0.00013
NM_000821.7(GGCX):c.*1604G>A rs140768153 0.00012
NM_000821.7(GGCX):c.*3393C>T rs868109874 0.00009
NM_000821.7(GGCX):c.*3581C>T rs1019659963 0.00009
NM_000821.7(GGCX):c.*3756A>G rs766023039 0.00009
NM_000821.7(GGCX):c.26G>A (p.Arg9Gln) rs745564526 0.00009
NM_000821.7(GGCX):c.507T>C (p.Phe169=) rs536257863 0.00009
NM_000821.7(GGCX):c.*285G>A rs893789215 0.00007
NM_000821.7(GGCX):c.*3841T>A rs986672098 0.00006
NM_000821.7(GGCX):c.*4397G>A rs564820085 0.00006
NM_000821.7(GGCX):c.990G>C (p.Leu330=) rs374754358 0.00006
NM_000821.7(GGCX):c.*218G>A rs772911409 0.00005
NM_000821.7(GGCX):c.*2892A>C rs146540264 0.00005
NM_000821.7(GGCX):c.1439+15C>T rs758719852 0.00005
NM_000821.7(GGCX):c.1492C>T (p.Arg498Cys) rs372161185 0.00005
NM_000821.7(GGCX):c.1299G>C (p.Gln433His) rs184476736 0.00004
NM_000821.7(GGCX):c.614G>A (p.Gly205Asp) rs749978184 0.00004
NM_000821.7(GGCX):c.*2716A>G rs901180216 0.00003
NM_000821.7(GGCX):c.*4215G>A rs886056358 0.00003
NM_000821.7(GGCX):c.*856T>C rs886056374 0.00003
NM_000821.7(GGCX):c.*2774A>G rs140009094 0.00002
NM_000821.7(GGCX):c.1224C>A (p.His408Gln) rs763288483 0.00002
NM_000821.7(GGCX):c.1249G>A (p.Asp417Asn) rs370517365 0.00002
NM_000821.7(GGCX):c.1815C>G (p.Asn605Lys) rs1375142657 0.00002
NM_000821.7(GGCX):c.57A>T (p.Lys19Asn) rs367575308 0.00002
NM_000821.7(GGCX):c.*199A>C rs1455293219 0.00001
NM_000821.7(GGCX):c.*2226C>T rs1002400857 0.00001
NM_000821.7(GGCX):c.*25T>C rs765806745 0.00001
NM_000821.7(GGCX):c.*2647T>C rs886056365 0.00001
NM_000821.7(GGCX):c.*2740A>C rs1184420625 0.00001
NM_000821.7(GGCX):c.*3177T>G rs1324933410 0.00001
NM_000821.7(GGCX):c.*3517T>C rs886056364 0.00001
NM_000821.7(GGCX):c.*3924A>G rs886056359 0.00001
NM_000821.7(GGCX):c.*4078G>A rs866533240 0.00001
NM_000821.7(GGCX):c.*703C>T rs867939864 0.00001
NM_000821.7(GGCX):c.1155+12C>A rs1284965933 0.00001
NM_000821.7(GGCX):c.1455T>C (p.Arg485=) rs1416935549 0.00001
NM_000821.7(GGCX):c.2012G>A (p.Arg671His) rs1350379349 0.00001
NM_000821.7(GGCX):c.269G>A (p.Arg90Gln) rs753656195 0.00001
NM_000821.7(GGCX):c.654G>A (p.Lys218=) rs774751096 0.00001
NM_000821.7(GGCX):c.903C>T (p.Tyr301=) rs751710756 0.00001
NM_000821.7(GGCX):c.*1019G>C rs545427723
NM_000821.7(GGCX):c.*1037A>G rs184378248
NM_000821.7(GGCX):c.*1145G>A rs1297390996
NM_000821.7(GGCX):c.*1186A>G rs886056372
NM_000821.7(GGCX):c.*1324T>C rs757965941
NM_000821.7(GGCX):c.*1686C>G rs1177037435
NM_000821.7(GGCX):c.*1712A>C rs557850002
NM_000821.7(GGCX):c.*1721G>A rs187452629
NM_000821.7(GGCX):c.*1727A>G rs114386392
NM_000821.7(GGCX):c.*1819A>C rs886056370
NM_000821.7(GGCX):c.*2299C>T rs886056368
NM_000821.7(GGCX):c.*2304T>C rs886056367
NM_000821.7(GGCX):c.*2560A>G rs886056366
NM_000821.7(GGCX):c.*2965C>A rs1340998302
NM_000821.7(GGCX):c.*3000A>G rs190910259
NM_000821.7(GGCX):c.*309A>G rs886056376
NM_000821.7(GGCX):c.*3630A>T rs886056363
NM_000821.7(GGCX):c.*3703C>T rs1691656620
NM_000821.7(GGCX):c.*3757T>C rs886056361
NM_000821.7(GGCX):c.*4047T>C rs189391524
NM_000821.7(GGCX):c.*417G>A rs768419574
NM_000821.7(GGCX):c.*4288G>C rs886056357
NM_000821.7(GGCX):c.*4366C>T rs550873302
NM_000821.7(GGCX):c.*4475T>C rs1691612144
NM_000821.7(GGCX):c.*610C>T rs532781606
NM_000821.7(GGCX):c.*680G>A rs139300235
NM_000821.7(GGCX):c.*91G>T rs1383100743
NM_000821.7(GGCX):c.*973A>G rs1691798044
NM_000821.7(GGCX):c.-23C>T rs537250931
NM_000821.7(GGCX):c.1008C>T (p.Ala336=) rs1692059799
NM_000821.7(GGCX):c.1046G>C (p.Arg349Pro) rs146930374
NM_000821.7(GGCX):c.1140dup (p.His381fs) rs1558807827
NM_000821.7(GGCX):c.1217G>A (p.Arg406His) rs139574592
NM_000821.7(GGCX):c.137C>T (p.Ser46Phe) rs201510718
NM_000821.7(GGCX):c.1453C>T (p.Arg485Cys) rs773659201
NM_000821.7(GGCX):c.1485C>T (p.Pro495=) rs1691972995
NM_000821.7(GGCX):c.198C>T (p.Val66=) rs147427088
NM_000821.7(GGCX):c.1994G>A (p.Arg665Lys) rs1691898500
NM_000821.7(GGCX):c.2119A>C (p.Ile707Leu) rs755087978
NM_000821.7(GGCX):c.2133T>G (p.Pro711=) rs886056379
NM_000821.7(GGCX):c.271A>C (p.Lys91Gln) rs1692323011
NM_000821.7(GGCX):c.68A>G (p.Glu23Gly) rs886056380
NM_000821.7(GGCX):c.726-4G>T rs146123760
NM_000821.7(GGCX):c.745C>T (p.Leu249=) rs1262224787
NM_000821.7(GGCX):c.994C>A (p.Pro332Thr) rs750270424

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