ClinVar Miner

List of variants in gene SZT2 reported as likely benign for epilepsy

Included ClinVar conditions (438):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 135
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HGVS dbSNP gnomAD frequency
NM_001365999.1(SZT2):c.2631C>T (p.Thr877=) rs140831372 0.00717
NM_001365999.1(SZT2):c.7573G>A (p.Val2525Ile) rs139486476 0.00717
NM_001365999.1(SZT2):c.4701G>A (p.Leu1567=) rs111932993 0.00598
NM_001365999.1(SZT2):c.8910C>T (p.Ser2970=) rs116536134 0.00441
NM_001365999.1(SZT2):c.5075C>T (p.Thr1692Ile) rs149831634 0.00427
NM_001365999.1(SZT2):c.4531G>A (p.Val1511Ile) rs76675748 0.00361
NM_001365999.1(SZT2):c.7562T>C (p.Val2521Ala) rs150113647 0.00337
NM_001365999.1(SZT2):c.8499+8A>C rs182225944 0.00297
NM_001365999.1(SZT2):c.6573C>T (p.Asp2191=) rs114046098 0.00267
NM_001365999.1(SZT2):c.9782G>A (p.Arg3261Gln) rs190363418 0.00207
NM_001365999.1(SZT2):c.7256G>A (p.Arg2419Gln) rs72637949 0.00103
NM_001365999.1(SZT2):c.7975-10C>T rs181831231 0.00100
NM_001365999.1(SZT2):c.4983T>C (p.Asp1661=) rs139810154 0.00098
NM_001365999.1(SZT2):c.8427G>A (p.Glu2809=) rs140309222 0.00088
NM_001365999.1(SZT2):c.9555C>T (p.His3185=) rs150150240 0.00079
NM_001365999.1(SZT2):c.9732G>A (p.Pro3244=) rs200250871 0.00066
NM_001365999.1(SZT2):c.1488G>A (p.Thr496=) rs370045267 0.00064
NM_001365999.1(SZT2):c.7641C>T (p.His2547=) rs144699351 0.00063
NM_001365999.1(SZT2):c.9201C>T (p.His3067=) rs114396679 0.00056
NM_001365999.1(SZT2):c.1791C>T (p.His597=) rs151110718 0.00055
NM_001365999.1(SZT2):c.8177C>G (p.Thr2726Ser) rs145882968 0.00055
NM_001365999.1(SZT2):c.3469C>T (p.Pro1157Ser) rs150966402 0.00054
NM_001365999.1(SZT2):c.9828C>T (p.Asp3276=) rs12756587 0.00046
NM_001365999.1(SZT2):c.5937C>T (p.His1979=) rs149717460 0.00038
NM_001365999.1(SZT2):c.6582A>G (p.Thr2194=) rs145802078 0.00038
NM_001365999.1(SZT2):c.2499C>T (p.Phe833=) rs777334279 0.00030
NM_001365999.1(SZT2):c.1335A>T (p.Ala445=) rs377411973 0.00027
NM_001365999.1(SZT2):c.1296G>A (p.Leu432=) rs769656441 0.00024
NM_001365999.1(SZT2):c.8148A>G (p.Glu2716=) rs199826167 0.00023
NM_001365999.1(SZT2):c.1458T>C (p.Arg486=) rs376484331 0.00021
NM_001365999.1(SZT2):c.528T>C (p.Pro176=) rs780340130 0.00021
NM_001365999.1(SZT2):c.8031G>A (p.Ala2677=) rs138303356 0.00019
NM_001365999.1(SZT2):c.2788C>T (p.Leu930=) rs148208657 0.00016
NM_001365999.1(SZT2):c.7224C>T (p.Asn2408=) rs373992628 0.00016
NM_001365999.1(SZT2):c.8316G>A (p.Thr2772=) rs532810601 0.00016
NM_001365999.1(SZT2):c.9795G>C (p.Leu3265=) rs569613488 0.00015
NM_001365999.1(SZT2):c.2034C>T (p.His678=) rs201529142 0.00014
NM_001365999.1(SZT2):c.4524G>A (p.Glu1508=) rs146416049 0.00014
NM_001365999.1(SZT2):c.8424G>A (p.Leu2808=) rs372935996 0.00013
NM_001365999.1(SZT2):c.7671C>T (p.Ile2557=) rs201311847 0.00012
NM_001365999.1(SZT2):c.9630C>T (p.Arg3210=) rs773985024 0.00012
NM_001365999.1(SZT2):c.3838G>A (p.Ala1280Thr) rs141075866 0.00011
NM_001365999.1(SZT2):c.5910G>C (p.Leu1970=) rs151260299 0.00011
NM_001365999.1(SZT2):c.6306C>G (p.Ser2102=) rs1009175468 0.00011
NM_001365999.1(SZT2):c.1881C>T (p.Phe627=) rs749921213 0.00010
NM_001365999.1(SZT2):c.3251C>T (p.Pro1084Leu) rs373408367 0.00009
NM_001365999.1(SZT2):c.5142C>T (p.Ile1714=) rs756050426 0.00009
NM_001365999.1(SZT2):c.8295C>T (p.Asp2765=) rs181686875 0.00009
NM_001365999.1(SZT2):c.8725C>T (p.Leu2909=) rs111662559 0.00009
NM_001365999.1(SZT2):c.6351C>T (p.Leu2117=) rs370166503 0.00008
NM_001365999.1(SZT2):c.7069T>C (p.Leu2357=) rs771086530 0.00008
NM_001365999.1(SZT2):c.2256-10C>T rs747740233 0.00007
NM_001365999.1(SZT2):c.3489G>A (p.Lys1163=) rs149793909 0.00007
NM_001365999.1(SZT2):c.9287-8T>C rs183871754 0.00007
NM_001365999.1(SZT2):c.1191C>T (p.Ala397=) rs772072313 0.00006
NM_001365999.1(SZT2):c.2409G>A (p.Pro803=) rs180810470 0.00006
NM_001365999.1(SZT2):c.3306C>T (p.Ser1102=) rs370803181 0.00006
NM_001365999.1(SZT2):c.390C>T (p.Gly130=) rs187131803 0.00006
NM_001365999.1(SZT2):c.4370T>A (p.Phe1457Tyr) rs147201727 0.00006
NM_001365999.1(SZT2):c.6738C>T (p.Leu2246=) rs374441368 0.00006
NM_001365999.1(SZT2):c.7479G>A (p.Ala2493=) rs751309639 0.00006
NM_001365999.1(SZT2):c.8556A>C (p.Thr2852=) rs201027552 0.00006
NM_001365999.1(SZT2):c.8817C>T (p.Pro2939=) rs777808688 0.00006
NM_001365999.1(SZT2):c.1797G>A (p.Pro599=) rs748420169 0.00005
NM_001365999.1(SZT2):c.6541C>T (p.Leu2181=) rs145034016 0.00005
NM_001365999.1(SZT2):c.7830T>G (p.Leu2610=) rs145125111 0.00005
NM_001365999.1(SZT2):c.1272A>G (p.Gln424=) rs780157180 0.00004
NM_001365999.1(SZT2):c.1395C>T (p.Gly465=) rs373535733 0.00004
NM_001365999.1(SZT2):c.3355C>G (p.Pro1119Ala) rs137956992 0.00004
NM_001365999.1(SZT2):c.4356C>T (p.Ser1452=) rs200813502 0.00004
NM_001365999.1(SZT2):c.4599C>T (p.Asp1533=) rs200228680 0.00004
NM_001365999.1(SZT2):c.4716C>T (p.Ser1572=) rs147043685 0.00004
NM_001365999.1(SZT2):c.546C>T (p.Phe182=) rs781292135 0.00004
NM_001365999.1(SZT2):c.6936G>A (p.Ala2312=) rs192791002 0.00004
NM_001365999.1(SZT2):c.835C>T (p.Leu279=) rs373897662 0.00004
NM_001365999.1(SZT2):c.8947C>T (p.Leu2983=) rs752431707 0.00004
NM_001365999.1(SZT2):c.9360T>C (p.Ser3120=) rs367855839 0.00004
NM_001365999.1(SZT2):c.9629G>A (p.Arg3210His) rs371193436 0.00004
NM_001365999.1(SZT2):c.10239C>T (p.Tyr3413=) rs757144339 0.00003
NM_001365999.1(SZT2):c.1107A>G (p.Leu369=) rs533632273 0.00003
NM_001365999.1(SZT2):c.2169A>T (p.Ser723=) rs1327247768 0.00003
NM_001365999.1(SZT2):c.2875C>T (p.Leu959=) rs1570647334 0.00003
NM_001365999.1(SZT2):c.3657C>T (p.Tyr1219=) rs111604978 0.00003
NM_001365999.1(SZT2):c.3690G>A (p.Ala1230=) rs1041324146 0.00003
NM_001365999.1(SZT2):c.429C>T (p.Ile143=) rs1209373381 0.00003
NM_001365999.1(SZT2):c.4419C>T (p.Asp1473=) rs377200944 0.00003
NM_001365999.1(SZT2):c.4710G>A (p.Thr1570=) rs375889333 0.00003
NM_001365999.1(SZT2):c.5052G>A (p.Thr1684=) rs776237704 0.00003
NM_001365999.1(SZT2):c.6060G>A (p.Ala2020=) rs141635115 0.00003
NM_001365999.1(SZT2):c.7317G>A (p.Ala2439=) rs372293082 0.00003
NM_001365999.1(SZT2):c.2775G>A (p.Lys925=) rs1055395161 0.00002
NM_001365999.1(SZT2):c.3243T>C (p.His1081=) rs200981894 0.00002
NM_001365999.1(SZT2):c.3810G>A (p.Gln1270=) rs1323463488 0.00002
NM_001365999.1(SZT2):c.3978G>A (p.Ala1326=) rs768548993 0.00002
NM_001365999.1(SZT2):c.4080T>C (p.Pro1360=) rs775980814 0.00002
NM_001365999.1(SZT2):c.5391G>A (p.Ala1797=) rs752230870 0.00002
NM_001365999.1(SZT2):c.5832G>A (p.Pro1944=) rs759851058 0.00002
NM_001365999.1(SZT2):c.6666G>C (p.Leu2222=) rs142775911 0.00002
NM_001365999.1(SZT2):c.7230G>A (p.Ser2410=) rs754459485 0.00002
NM_001365999.1(SZT2):c.1302A>G (p.Lys434=) rs1420992888 0.00001
NM_001365999.1(SZT2):c.2220G>A (p.Val740=) rs576623885 0.00001
NM_001365999.1(SZT2):c.2427G>A (p.Ala809=) rs761742264 0.00001
NM_001365999.1(SZT2):c.6084A>C (p.Thr2028=) rs1366420391 0.00001
NM_001365999.1(SZT2):c.6816C>T (p.Gly2272=) rs150870098 0.00001
NM_001365999.1(SZT2):c.7389T>C (p.Asp2463=) rs778123763 0.00001
NM_001365999.1(SZT2):c.7896C>T (p.Phe2632=) rs773642457 0.00001
NM_001365999.1(SZT2):c.8013G>A (p.Gly2671=) rs765145256 0.00001
NM_001365999.1(SZT2):c.8125T>C (p.Leu2709=) rs761871479 0.00001
NM_001365999.1(SZT2):c.8280C>T (p.Asp2760=) rs1186640842 0.00001
NM_001365999.1(SZT2):c.8430C>T (p.Arg2810=) rs377123278 0.00001
NM_001365999.1(SZT2):c.900T>C (p.Tyr300=) rs748111311 0.00001
NM_001365999.1(SZT2):c.9330A>G (p.Leu3110=) rs749144612 0.00001
NM_001365999.1(SZT2):c.9486C>T (p.Asp3162=) rs749826900 0.00001
NM_001365999.1(SZT2):c.10002C>T (p.Tyr3334=)
NM_001365999.1(SZT2):c.1488G>T (p.Thr496=) rs370045267
NM_001365999.1(SZT2):c.1770-11C>T rs756655876
NM_001365999.1(SZT2):c.2208G>T (p.Arg736=) rs904037938
NM_001365999.1(SZT2):c.2356C>T (p.Leu786=) rs878855007
NM_001365999.1(SZT2):c.2412A>C (p.Ser804=) rs2153932904
NM_001365999.1(SZT2):c.2471+8A>T rs754795755
NM_001365999.1(SZT2):c.2916G>T (p.Pro972=) rs758017419
NM_001365999.1(SZT2):c.3345C>T (p.Ile1115=) rs775988619
NM_001365999.1(SZT2):c.4525C>T (p.Leu1509=) rs1557566670
NM_001365999.1(SZT2):c.4817G>A (p.Arg1606Gln)
NM_001365999.1(SZT2):c.4915C>A (p.Arg1639=) rs753322092
NM_001365999.1(SZT2):c.4995G>T (p.Gly1665=) rs1653847013
NM_001365999.1(SZT2):c.5379G>A (p.Glu1793=) rs765099450
NM_001365999.1(SZT2):c.5517C>T (p.Arg1839=) rs147753139
NM_001365999.1(SZT2):c.5766G>C (p.Arg1922=) rs760518748
NM_001365999.1(SZT2):c.6039T>C (p.Tyr2013=) rs1192938717
NM_001365999.1(SZT2):c.603G>A (p.Leu201=) rs1557531678
NM_001365999.1(SZT2):c.7230G>T (p.Ser2410=) rs754459485
NM_001365999.1(SZT2):c.7446G>A (p.Glu2482=) rs979339741
NM_001365999.1(SZT2):c.7874-16C>G rs72883828
NM_001365999.1(SZT2):c.9339C>T (p.Tyr3113=)

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