ClinVar Miner

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

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_001040142.2(SCN2A):c.100G>A (p.Ala34Thr) rs144814658
NM_001040142.2(SCN2A):c.1095G>A (p.Thr365=) rs2227900
NM_001040142.2(SCN2A):c.1177-8T>C rs1060504831
NM_001040142.2(SCN2A):c.1384-4C>G rs113191507
NM_001040142.2(SCN2A):c.1386G>A (p.Ala462=) rs145912536
NM_001040142.2(SCN2A):c.1416A>G (p.Arg472=) rs200246820
NM_001040142.2(SCN2A):c.1536A>G (p.Glu512=) rs201680546
NM_001040142.2(SCN2A):c.1571G>A (p.Arg524Gln) rs186154973
NM_001040142.2(SCN2A):c.1605A>G (p.Lys535=) rs367647572
NM_001040142.2(SCN2A):c.1842G>A (p.Pro614=) rs114315466
NM_001040142.2(SCN2A):c.1923T>C (p.Asn641=) rs780183614
NM_001040142.2(SCN2A):c.1938C>T (p.Ser646=) rs528391611
NM_001040142.2(SCN2A):c.1976G>A (p.Gly659Asp) rs368887417
NM_001040142.2(SCN2A):c.2304C>T (p.Cys768=) rs764479273
NM_001040142.2(SCN2A):c.24G>A (p.Pro8=) rs149534277
NM_001040142.2(SCN2A):c.2562+5A>G rs374738441
NM_001040142.2(SCN2A):c.2661A>G (p.Val887=) rs749540280
NM_001040142.2(SCN2A):c.2811C>T (p.Arg937=) rs779791354
NM_001040142.2(SCN2A):c.2919+8G>A rs552318566
NM_001040142.2(SCN2A):c.3261G>T (p.Val1087=) rs932319701
NM_001040142.2(SCN2A):c.3330A>C (p.Gly1110=) rs138143967
NM_001040142.2(SCN2A):c.3579C>A (p.Leu1193=) rs367546924
NM_001040142.2(SCN2A):c.3624T>C (p.Asn1208=) rs552725434
NM_001040142.2(SCN2A):c.3975T>G (p.Val1325=) rs1553593569
NM_001040142.2(SCN2A):c.4224A>G (p.Val1408=) rs1060504830
NM_001040142.2(SCN2A):c.4257C>T (p.Ala1419=) rs141153302
NM_001040142.2(SCN2A):c.4260G>A (p.Thr1420=) rs138241682
NM_001040142.2(SCN2A):c.4287T>C (p.Tyr1429=) rs150209984
NM_001040142.2(SCN2A):c.432A>G (p.Val144=) rs757533588
NM_001040142.2(SCN2A):c.4565G>C (p.Gly1522Ala) rs147522594
NM_001040142.2(SCN2A):c.4656C>T (p.Thr1552=) rs765041838
NM_001040142.2(SCN2A):c.5155T>C (p.Leu1719=) rs199698414
NM_001040142.2(SCN2A):c.5397T>C (p.Tyr1799=) rs200603552
NM_001040142.2(SCN2A):c.5468A>C (p.Asp1823Ala) rs138497939
NM_001040142.2(SCN2A):c.5517C>T (p.Leu1839=) rs148424455
NM_001040142.2(SCN2A):c.5541G>A (p.Val1847=) rs371704720
NM_001040142.2(SCN2A):c.5721G>T (p.Val1907=) rs1060504829
NM_001040142.2(SCN2A):c.5760C>T (p.Leu1920=) rs1449263336
NM_001040142.2(SCN2A):c.5955A>G (p.Lys1985=) rs572474239
NM_001040142.2(SCN2A):c.879T>G (p.Thr293=) rs201685102

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