ClinVar Miner

List of variants in gene SCN2A reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 121
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HGVS dbSNP
NM_001040142.2(SCN2A):c.*9C>A rs541483828
NM_001040142.2(SCN2A):c.-41T>C rs777439927
NM_001040142.2(SCN2A):c.-51-136C>T
NM_001040142.2(SCN2A):c.-51-1657G>T rs962697383
NM_001040142.2(SCN2A):c.-51-1658G>T rs796053109
NM_001040142.2(SCN2A):c.-51-61A>G
NM_001040142.2(SCN2A):c.100G>A (p.Ala34Thr) rs144814658
NM_001040142.2(SCN2A):c.1035-113C>T
NM_001040142.2(SCN2A):c.1038G>A (p.Gln346=) rs1057522529
NM_001040142.2(SCN2A):c.1177-15T>G rs1398497493
NM_001040142.2(SCN2A):c.1177-16C>G rs553983883
NM_001040142.2(SCN2A):c.1200G>T (p.Thr400=) rs532681917
NM_001040142.2(SCN2A):c.1306T>C (p.Leu436=) rs376323449
NM_001040142.2(SCN2A):c.1383+20G>A rs567354567
NM_001040142.2(SCN2A):c.1384-4C>G rs113191507
NM_001040142.2(SCN2A):c.1386G>A (p.Ala462=) rs145912536
NM_001040142.2(SCN2A):c.1389A>G (p.Ala463=) rs9333575
NM_001040142.2(SCN2A):c.1402_1404del (p.Ser468del) rs780584405
NM_001040142.2(SCN2A):c.1599A>G (p.Arg533=) rs1553569785
NM_001040142.2(SCN2A):c.1671+45A>T
NM_001040142.2(SCN2A):c.1671+64T>C
NM_001040142.2(SCN2A):c.1672-7T>C rs1553571855
NM_001040142.2(SCN2A):c.1759A>C (p.Ile587Leu) rs148275498
NM_001040142.2(SCN2A):c.1833G>A (p.Leu611=) rs1057522258
NM_001040142.2(SCN2A):c.1836C>T (p.Phe612=)
NM_001040142.2(SCN2A):c.1866C>T (p.His622=) rs377388875
NM_001040142.2(SCN2A):c.1938C>T (p.Ser646=) rs528391611
NM_001040142.2(SCN2A):c.1953T>C (p.Asn651=) rs199722574
NM_001040142.2(SCN2A):c.1984A>G (p.Thr662Ala) rs796053111
NM_001040142.2(SCN2A):c.2016+10A>G rs886042771
NM_001040142.2(SCN2A):c.2016+120G>A
NM_001040142.2(SCN2A):c.2017-9T>C rs1451143110
NM_001040142.2(SCN2A):c.2050C>T (p.Arg684Trp) rs200783308
NM_001040142.2(SCN2A):c.2079T>C (p.Asp693=) rs1553573107
NM_001040142.2(SCN2A):c.2083T>C (p.Leu695=) rs368043574
NM_001040142.2(SCN2A):c.2149+136C>T
NM_001040142.2(SCN2A):c.2150-10T>G rs1057523367
NM_001040142.2(SCN2A):c.2150-236A>G
NM_001040142.2(SCN2A):c.2157A>G (p.Glu719=) rs779574574
NM_001040142.2(SCN2A):c.2304C>T (p.Cys768=) rs764479273
NM_001040142.2(SCN2A):c.2352G>A (p.Thr784=) rs369101059
NM_001040142.2(SCN2A):c.2386C>T (p.Leu796=)
NM_001040142.2(SCN2A):c.2388+126G>A
NM_001040142.2(SCN2A):c.2388+12T>C rs749226972
NM_001040142.2(SCN2A):c.2388+6C>A
NM_001040142.2(SCN2A):c.2389G>A (p.Val797Ile) rs142128956
NM_001040142.2(SCN2A):c.2518T>C (p.Leu840=) rs768817318
NM_001040142.2(SCN2A):c.252C>T (p.Tyr84=) rs143065769
NM_001040142.2(SCN2A):c.2541A>T (p.Ser847=) rs776618474
NM_001040142.2(SCN2A):c.2563-4C>A rs561375550
NM_001040142.2(SCN2A):c.2637G>C (p.Gly879=) rs1490972796
NM_001040142.2(SCN2A):c.267+292C>T
NM_001040142.2(SCN2A):c.2673C>T (p.Ile891=) rs529842407
NM_001040142.2(SCN2A):c.268-19G>A rs898178511
NM_001040142.2(SCN2A):c.270G>A (p.Thr90=) rs776081713
NM_001040142.2(SCN2A):c.2757A>G (p.Glu919=) rs1057520595
NM_001040142.2(SCN2A):c.2760C>T (p.Leu920=) rs1057523075
NM_001040142.2(SCN2A):c.2919+16A>G rs1343240110
NM_001040142.2(SCN2A):c.3015T>C (p.Ile1005=) rs758652224
NM_001040142.2(SCN2A):c.3123G>A (p.Pro1041=) rs147576541
NM_001040142.2(SCN2A):c.3210C>T (p.Asp1070=) rs187731029
NM_001040142.2(SCN2A):c.3255T>C (p.Tyr1085=) rs1057521230
NM_001040142.2(SCN2A):c.3330A>C (p.Gly1110=) rs138143967
NM_001040142.2(SCN2A):c.3399+14A>C rs376371059
NM_001040142.2(SCN2A):c.3435G>A (p.Thr1145=) rs1345931602
NM_001040142.2(SCN2A):c.3457G>A (p.Glu1153Lys) rs200138205
NM_001040142.2(SCN2A):c.3520+11C>T rs187452739
NM_001040142.2(SCN2A):c.3520+327A>C
NM_001040142.2(SCN2A):c.3521-12C>T rs370419172
NM_001040142.2(SCN2A):c.3675+9T>C
NM_001040142.2(SCN2A):c.3676-20T>C rs1057522535
NM_001040142.2(SCN2A):c.3702G>A (p.Gln1234=) rs1198199936
NM_001040142.2(SCN2A):c.3850-231G>A
NM_001040142.2(SCN2A):c.3850-40T>C
NM_001040142.2(SCN2A):c.3850-92C>T
NM_001040142.2(SCN2A):c.3852C>T (p.Val1284=) rs1057521569
NM_001040142.2(SCN2A):c.3921A>G (p.Thr1307=)
NM_001040142.2(SCN2A):c.3939A>G (p.Pro1313=) rs1553593075
NM_001040142.2(SCN2A):c.3973-268G>A
NM_001040142.2(SCN2A):c.4045C>T (p.Leu1349=) rs946393942
NM_001040142.2(SCN2A):c.4221C>T (p.Asn1407=) rs747792907
NM_001040142.2(SCN2A):c.4254+233A>G
NM_001040142.2(SCN2A):c.4260G>A (p.Thr1420=) rs138241682
NM_001040142.2(SCN2A):c.4308+282T>C
NM_001040142.2(SCN2A):c.4309-10T>C rs1057522929
NM_001040142.2(SCN2A):c.432A>G (p.Val144=) rs757533588
NM_001040142.2(SCN2A):c.4447-6C>T rs1173151782
NM_001040142.2(SCN2A):c.4461C>T (p.Asp1487=) rs1553462203
NM_001040142.2(SCN2A):c.4539A>T (p.Ile1513=) rs200553623
NM_001040142.2(SCN2A):c.4552-14A>G rs775130301
NM_001040142.2(SCN2A):c.4565G>C (p.Gly1522Ala) rs147522594
NM_001040142.2(SCN2A):c.4823-15G>T rs375524288
NM_001040142.2(SCN2A):c.4854T>C (p.Tyr1618=) rs770349641
NM_001040142.2(SCN2A):c.4860G>A (p.Val1620=) rs369939991
NM_001040142.2(SCN2A):c.489A>G (p.Thr163=) rs1057520898
NM_001040142.2(SCN2A):c.4944G>A (p.Thr1648=) rs565309819
NM_001040142.2(SCN2A):c.5121G>A (p.Leu1707=) rs377063535
NM_001040142.2(SCN2A):c.5127A>G (p.Gln1709=) rs938025387
NM_001040142.2(SCN2A):c.5155T>C (p.Leu1719=) rs199698414
NM_001040142.2(SCN2A):c.5166T>C (p.Pro1722=) rs760587370
NM_001040142.2(SCN2A):c.5217A>C (p.Gly1739=) rs2227899
NM_001040142.2(SCN2A):c.5319G>A (p.Ala1773=) rs373913233
NM_001040142.2(SCN2A):c.5364G>A (p.Glu1788=) rs199925238
NM_001040142.2(SCN2A):c.5446G>T (p.Ala1816Ser) rs147084515
NM_001040142.2(SCN2A):c.5468A>C (p.Asp1823Ala) rs138497939
NM_001040142.2(SCN2A):c.5574A>G (p.Leu1858=) rs767592553
NM_001040142.2(SCN2A):c.5580T>G (p.Ala1860=) rs752845880
NM_001040142.2(SCN2A):c.5697G>A (p.Thr1899=) rs746574956
NM_001040142.2(SCN2A):c.5817A>G (p.Glu1939=) rs780514937
NM_001040142.2(SCN2A):c.605+13A>G rs1553567417
NM_001040142.2(SCN2A):c.605+15_605+16delinsTATT rs1553567419
NM_001040142.2(SCN2A):c.672A>G (p.Ala224=) rs2228986
NM_001040142.2(SCN2A):c.681A>C (p.Thr227=) rs2228987
NM_001040142.2(SCN2A):c.698-20C>T rs748075978
NM_001040142.2(SCN2A):c.70G>A (p.Ala24Thr) rs527452801
NM_001040142.2(SCN2A):c.82C>T (p.Arg28Cys) rs200884216
NM_001040142.2(SCN2A):c.879T>G (p.Thr293=) rs201685102
NM_001040142.2(SCN2A):c.952G>A (p.Glu318Lys) rs149987700
NM_001040142.2(SCN2A):c.960T>C (p.Ile320=) rs185590667
NM_001040142.2(SCN2A):c.982T>G (p.Phe328Val) rs781204054
NM_021007.2(SCN2A):c.-51-16dupC rs1325277297

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