ClinVar Miner

List of variants in gene MAP2K2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP gnomAD frequency
NM_030662.4(MAP2K2):c.92+266G>A rs192871074 0.01343
NM_030662.4(MAP2K2):c.705+128C>T rs56120956 0.01303
NM_030662.4(MAP2K2):c.304-127G>A rs138469122 0.01015
NM_030662.4(MAP2K2):c.1046+200C>T rs116476767 0.00928
NC_000019.10:g.4124295C>T rs567625341 0.00888
NM_030662.4(MAP2K2):c.450+307C>A rs62132103 0.00790
NM_030662.4(MAP2K2):c.1092+127G>A rs116693958 0.00755
NM_030662.4(MAP2K2):c.1046+303del rs574248280 0.00753
NM_030662.4(MAP2K2):c.1093-128G>A rs188271658 0.00677
NM_030662.4(MAP2K2):c.450+40C>T rs140556662 0.00581
NM_030662.4(MAP2K2):c.528+26C>T rs73918027 0.00506
NM_030662.4(MAP2K2):c.1047-212G>A rs559885829 0.00364
NM_030662.4(MAP2K2):c.1047-31G>A rs181512820 0.00329
NM_030662.3(MAP2K2):c.-419C>A rs144939535 0.00300
NM_030662.3(MAP2K2):c.-406C>A rs149141097 0.00297
NM_030662.4(MAP2K2):c.304-46G>A rs112996316 0.00049
NM_030662.4(MAP2K2):c.529-27C>A rs371369471 0.00036
NM_030662.4(MAP2K2):c.1191C>T (p.Arg397=) rs148592592 0.00031
NM_030662.4(MAP2K2):c.303+29G>A rs180919929 0.00024
NM_030662.4(MAP2K2):c.450+17C>T rs199892711 0.00021
NM_030662.4(MAP2K2):c.919+10G>A rs780890887 0.00018
NM_030662.4(MAP2K2):c.580+15G>A rs370921720 0.00014
NM_030662.4(MAP2K2):c.784G>A (p.Val262Ile) rs138873805 0.00014
NM_030662.4(MAP2K2):c.581-8G>A rs369262004 0.00012
NM_030662.4(MAP2K2):c.580+14C>T rs544557960 0.00009
NM_030662.4(MAP2K2):c.894G>A (p.Pro298=) rs374526051 0.00009
NM_030662.4(MAP2K2):c.919+4C>T rs763424788 0.00009
NM_030662.4(MAP2K2):c.258C>A (p.Val86=) rs148437150 0.00008
NM_030662.4(MAP2K2):c.853G>A (p.Asp285Asn) rs150369301 0.00008
NM_030662.4(MAP2K2):c.450+12C>T rs750513646 0.00007
NM_030662.4(MAP2K2):c.529-14G>A rs756414078 0.00007
NM_030662.4(MAP2K2):c.*20G>A rs377441764 0.00006
NM_030662.4(MAP2K2):c.1112G>A (p.Arg371Gln) rs730880514 0.00006
NM_030662.4(MAP2K2):c.450+20G>A rs374143146 0.00006
NM_030662.4(MAP2K2):c.451-7C>T rs780396876 0.00006
NM_030662.4(MAP2K2):c.536G>A (p.Arg179Gln) rs776316565 0.00005
NM_030662.4(MAP2K2):c.240G>A (p.Ala80=) rs543217722 0.00004
NM_030662.4(MAP2K2):c.456C>T (p.Gly152=) rs143106439 0.00004
NM_030662.4(MAP2K2):c.528+11C>T rs369913089 0.00004
NM_030662.4(MAP2K2):c.889C>T (p.Arg297Trp) rs562352756 0.00004
NM_030662.4(MAP2K2):c.93-6C>T rs727504836 0.00004
NM_030662.4(MAP2K2):c.1176C>T (p.Pro392=) rs529064753 0.00003
NM_030662.4(MAP2K2):c.1182A>G (p.Thr394=) rs375253105 0.00003
NM_030662.4(MAP2K2):c.304-7C>T rs561127903 0.00003
NM_030662.4(MAP2K2):c.581-3C>T rs754233409 0.00003
NM_030662.4(MAP2K2):c.581-9C>T rs539611844 0.00003
NM_030662.4(MAP2K2):c.705+10C>T rs372898071 0.00003
NM_030662.4(MAP2K2):c.818A>G (p.Lys273Arg) rs539555837 0.00003
NM_030662.4(MAP2K2):c.884C>T (p.Ser295Leu) rs531584619 0.00003
NM_030662.4(MAP2K2):c.1197C>T (p.Ala399=) rs987393686 0.00002
NM_030662.4(MAP2K2):c.327G>A (p.Pro109=) rs369156025 0.00002
NM_030662.4(MAP2K2):c.450+22G>A rs767239143 0.00002
NM_030662.4(MAP2K2):c.474G>A (p.Val158=) rs370736371 0.00002
NM_030662.4(MAP2K2):c.529-10T>C rs551098822 0.00002
NM_030662.4(MAP2K2):c.924C>T (p.His308=) rs768099163 0.00002
NM_030662.4(MAP2K2):c.952A>G (p.Ile318Val) rs1064797064 0.00002
NM_030662.4(MAP2K2):c.*2A>T rs1057521556 0.00001
NM_030662.4(MAP2K2):c.1046+16C>A rs906888337 0.00001
NM_030662.4(MAP2K2):c.1085T>C (p.Met362Thr) rs730880513 0.00001
NM_030662.4(MAP2K2):c.1092A>G (p.Thr364=) rs779378237 0.00001
NM_030662.4(MAP2K2):c.1167G>A (p.Leu389=) rs1473228474 0.00001
NM_030662.4(MAP2K2):c.168C>T (p.Ala56=) rs147814905 0.00001
NM_030662.4(MAP2K2):c.207C>T (p.Asp69=) rs199850535 0.00001
NM_030662.4(MAP2K2):c.238G>A (p.Ala80Thr) rs751795549 0.00001
NM_030662.4(MAP2K2):c.581-11G>A rs758442973 0.00001
NM_030662.4(MAP2K2):c.639C>T (p.Phe213=) rs727504818 0.00001
NM_030662.4(MAP2K2):c.810C>T (p.Pro270=) rs374119774 0.00001
NM_030662.4(MAP2K2):c.814G>A (p.Ala272Thr) rs757240576 0.00001
NM_030662.4(MAP2K2):c.912C>T (p.Pro304=) rs1006127521 0.00001
NM_030662.4(MAP2K2):c.*14C>T rs374728969
NM_030662.4(MAP2K2):c.1046+91_1046+92del rs559885397
NM_030662.4(MAP2K2):c.1047-2dup rs1555696233
NM_030662.4(MAP2K2):c.1093-273C>T rs140520358
NM_030662.4(MAP2K2):c.258C>T (p.Val86=) rs148437150
NM_030662.4(MAP2K2):c.291C>G (p.Ile97Met) rs200918323
NM_030662.4(MAP2K2):c.303+15del rs758256765
NM_030662.4(MAP2K2):c.303+92_303+128del rs541009313
NM_030662.4(MAP2K2):c.351C>G (p.Arg117=) rs777670871
NM_030662.4(MAP2K2):c.581-19C>T rs573730409
NM_030662.4(MAP2K2):c.581-20C>T rs1057523179
NM_030662.4(MAP2K2):c.706-17C>T rs754737193
NM_030662.4(MAP2K2):c.806C>G (p.Pro269Arg) rs368064728
NM_030662.4(MAP2K2):c.860AAG[1] (p.Glu288del) rs763469132
NM_030662.4(MAP2K2):c.919+10_919+12delinsAAG rs1064794489
NM_030662.4(MAP2K2):c.920-17T>A rs1057524145

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