ClinVar Miner

List of variants in gene PLCG2 reported as benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_002661.5(PLCG2):c.2055-8T>C rs12448130 0.99057
NM_002661.5(PLCG2):c.3314-23C>A rs4405546 0.91524
NM_002661.5(PLCG2):c.1467+38G>C rs4435248 0.75887
NM_002661.5(PLCG2):c.431+37G>C rs4341734 0.74893
NM_002661.5(PLCG2):c.1497C>T (p.Ala499=) rs1143689 0.72851
NM_002661.5(PLCG2):c.174T>C (p.Ala58=) rs1143685 0.68306
NM_002661.5(PLCG2):c.432-13T>A rs4888183 0.55511
NM_002661.5(PLCG2):c.480-22A>G rs12445580 0.54348
NM_002661.5(PLCG2):c.2236-14C>G rs12446127 0.48966
NM_002661.5(PLCG2):c.3093T>C (p.Asn1031=) rs1071644 0.39075
NM_002661.5(PLCG2):c.1149C>T (p.Asp383=) rs1143688 0.33340
NM_002661.5(PLCG2):c.692+25C>T rs11865395 0.28270
NM_002661.5(PLCG2):c.297A>G (p.Leu99=) rs1143686 0.26621
NM_002661.5(PLCG2):c.1188C>G (p.Thr396=) rs13333716 0.06770
NM_002661.5(PLCG2):c.802C>T (p.Arg268Trp) rs1143687 0.04677
NM_002661.5(PLCG2):c.2916C>T (p.Val972=) rs1143690 0.03426
NM_002661.5(PLCG2):c.868-18C>T rs112707234 0.03249
NM_002661.5(PLCG2):c.565-10A>G rs62046684 0.03201
NM_002661.5(PLCG2):c.2054+7G>A rs138158454 0.02918
NM_002661.5(PLCG2):c.731A>G (p.His244Arg) rs11548656 0.02717
NM_002661.5(PLCG2):c.770A>T (p.His257Leu) rs45443101 0.02615
NM_002661.5(PLCG2):c.1558-18C>T rs113312523 0.01465
NM_002661.5(PLCG2):c.2418-16C>T rs116282799 0.01091
NM_002661.5(PLCG2):c.2514G>A (p.Gln838=) rs115583707 0.01090
NM_002661.5(PLCG2):c.82A>T (p.Met28Leu) rs61749044 0.00973
NM_002661.5(PLCG2):c.3482-3C>T rs74856898 0.00935
NM_002661.5(PLCG2):c.3726C>A (p.Leu1242=) rs76506409 0.00926
NM_002661.5(PLCG2):c.2262C>T (p.Asp754=) rs74032923 0.00884
NM_002661.5(PLCG2):c.3125G>C (p.Ser1042Thr) rs114262189 0.00831
NM_002661.5(PLCG2):c.1712A>G (p.Asn571Ser) rs75472618 0.00802
NM_002661.5(PLCG2):c.1146T>C (p.Phe382=) rs138637229 0.00731
NM_002661.5(PLCG2):c.2094C>T (p.Asp698=) rs143195637 0.00513
NM_002661.5(PLCG2):c.2542C>T (p.Leu848Phe) rs114618894 0.00510
NM_002661.5(PLCG2):c.1565C>G (p.Pro522Arg) rs72824905 0.00491
NM_002661.5(PLCG2):c.1444T>C (p.Tyr482His) rs187956469 0.00341
NM_002661.5(PLCG2):c.2161G>A (p.Glu721Lys) rs187454354 0.00333
NM_002661.5(PLCG2):c.2355C>T (p.Ser785=) rs185307548 0.00307
NM_002661.5(PLCG2):c.600A>G (p.Glu200=) rs142140333 0.00294
NM_002661.5(PLCG2):c.3414A>G (p.Glu1138=) rs61755443 0.00247
NM_002661.5(PLCG2):c.714C>T (p.Ala238=) rs138981519 0.00237
NM_002661.5(PLCG2):c.1557+6G>C rs139565830 0.00235
NM_002661.5(PLCG2):c.1152C>T (p.Asp384=) rs13333713 0.00222
NM_002661.5(PLCG2):c.1050C>A (p.Arg350=) rs185739725 0.00212
NM_002661.5(PLCG2):c.2324A>G (p.Lys775Arg) rs142825971 0.00204
NM_002661.5(PLCG2):c.987G>A (p.Thr329=) rs200506549 0.00164
NM_002661.5(PLCG2):c.2011A>G (p.Ile671Val) rs150833842 0.00157
NM_002661.5(PLCG2):c.2837A>G (p.Asn946Ser) rs139462941 0.00148
NM_002661.5(PLCG2):c.1533G>C (p.Gln511His) rs151013036 0.00131
NM_002661.5(PLCG2):c.3573G>A (p.Glu1191=) rs201682723 0.00128
NM_002661.5(PLCG2):c.1671G>A (p.Lys557=) rs372347274 0.00111
NM_002661.5(PLCG2):c.923C>T (p.Ala308Val) rs199636472 0.00104
NM_002661.5(PLCG2):c.771T>C (p.His257=) rs369555285 0.00091
NM_002661.5(PLCG2):c.1859C>T (p.Thr620Met) rs147396004 0.00084
NM_002661.5(PLCG2):c.2515-14T>G rs201412321 0.00067
NM_002661.5(PLCG2):c.3112C>T (p.Leu1038=) rs200813182 0.00067
NM_002661.5(PLCG2):c.57G>A (p.Lys19=) rs369542354 0.00055
NM_002661.5(PLCG2):c.1107C>T (p.Val369=) rs201652976 0.00041
NM_002661.5(PLCG2):c.2054+11G>C rs372245323 0.00041
NM_002661.5(PLCG2):c.579C>G (p.His193Gln) rs201080992 0.00041
NM_002661.5(PLCG2):c.2778C>T (p.Ile926=) rs371069005 0.00039
NM_002661.5(PLCG2):c.1959C>T (p.Arg653=) rs117835631 0.00035
NM_002661.5(PLCG2):c.1156G>A (p.Val386Met) rs769180169 0.00034
NM_002661.5(PLCG2):c.3198+20C>G rs141049260 0.00032
NM_002661.5(PLCG2):c.2739+8C>A rs201659233 0.00030
NM_002661.5(PLCG2):c.2655G>A (p.Pro885=) rs187441573 0.00029
NM_002661.5(PLCG2):c.648+12C>G rs145838332 0.00027
NM_002661.5(PLCG2):c.2658G>A (p.Val886=) rs549242688 0.00023
NM_002661.5(PLCG2):c.766-13T>G rs115570507 0.00022
NM_002661.5(PLCG2):c.1812C>T (p.Asn604=) rs191668546 0.00015
NM_002661.5(PLCG2):c.533G>A (p.Ser178Asn) rs200981336 0.00015
NM_002661.5(PLCG2):c.1014C>T (p.Ser338=) rs200149635 0.00014
NM_002661.5(PLCG2):c.2148C>T (p.Leu716=) rs367677388 0.00014
NM_002661.5(PLCG2):c.3053-19C>T rs202166689 0.00014
NM_002661.5(PLCG2):c.1383A>G (p.Arg461=) rs369098550 0.00013
NM_002661.5(PLCG2):c.1569T>A (p.Pro523=) rs199708049 0.00013
NM_002661.5(PLCG2):c.1467+20C>T rs370477719 0.00010
NM_002661.5(PLCG2):c.2259C>T (p.Tyr753=) rs370847174 0.00006
NM_002661.5(PLCG2):c.432-14A>G rs750581048 0.00005
NM_002661.5(PLCG2):c.1073-8C>G rs372603106 0.00004
NM_002661.5(PLCG2):c.1258G>A (p.Ala420Thr) rs201490178 0.00004
NM_002661.5(PLCG2):c.2055-20C>A rs563045009 0.00004
NM_002661.5(PLCG2):c.2478C>T (p.Asp826=) rs774618541 0.00004
NM_002661.5(PLCG2):c.2784C>T (p.Ile928=) rs769310647 0.00003
NM_002661.5(PLCG2):c.577C>G (p.His193Asp) rs1032603937 0.00001
NM_002661.5(PLCG2):c.1194-18A>G
NM_002661.5(PLCG2):c.1386C>G (p.Gly462=) rs759622571
NM_002661.5(PLCG2):c.1733+12G>C
NM_002661.5(PLCG2):c.1935-14G>T rs55645129
NM_002661.5(PLCG2):c.2236-14C>T rs12446127
NM_002661.5(PLCG2):c.2236-5dup
NM_002661.5(PLCG2):c.3052+10G>A
NM_002661.5(PLCG2):c.324G>C (p.Thr108=) rs189282309
NM_002661.5(PLCG2):c.479+22dup
NM_002661.5(PLCG2):c.540C>G (p.Ala180=) rs150276286
NM_002661.5(PLCG2):c.565-22del rs34761601
NM_002661.5(PLCG2):c.692+12C>G
NM_002661.5(PLCG2):c.867+12G>A

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