ClinVar Miner

List of variants in gene BICD2 reported as benign for peripheral neuropathy

Included ClinVar conditions (517):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_001003800.2(BICD2):c.1063-111G>C rs56339669 0.26288
NM_001003800.2(BICD2):c.2258+15G>C rs140501870 0.00450
NM_001003800.2(BICD2):c.269A>G (p.Lys90Arg) rs61754130 0.00437
NM_001003800.2(BICD2):c.2445G>A (p.Pro815=) rs34451610 0.00337
NM_001003800.2(BICD2):c.454-19T>C rs114997314 0.00256
NM_001003800.2(BICD2):c.1806G>A (p.Thr602=) rs138300993 0.00118
NM_001003800.2(BICD2):c.1387C>T (p.Arg463Cys) rs78319441 0.00113
NM_001003800.2(BICD2):c.240+8G>T rs371559371 0.00113
NM_001003800.2(BICD2):c.813C>T (p.Phe271=) rs150389188 0.00086
NM_001003800.2(BICD2):c.240+20C>A rs556051421 0.00083
NM_001003800.2(BICD2):c.72C>G (p.Ala24=) rs545512590 0.00078
NM_001003800.2(BICD2):c.2397C>T (p.Leu799=) rs151133287 0.00061
NM_001003800.2(BICD2):c.1348C>T (p.Arg450Cys) rs201997144 0.00058
NM_001003800.2(BICD2):c.1050G>A (p.Gln350=) rs368860496 0.00044
NM_001003800.2(BICD2):c.2012C>T (p.Ala671Val) rs200086216 0.00040
NM_001003800.2(BICD2):c.454-7C>G rs186469385 0.00040
NM_001003800.2(BICD2):c.861C>T (p.Asp287=) rs768173580 0.00036
NM_001003800.2(BICD2):c.1842A>G (p.Pro614=) rs200912578 0.00024
NM_001003800.2(BICD2):c.1192C>T (p.Arg398Trp) rs189266003 0.00020
NM_001003800.2(BICD2):c.1044G>A (p.Leu348=) rs77530912 0.00017
NM_001003800.2(BICD2):c.1539C>T (p.Ala513=) rs369575401 0.00016
NM_001003800.2(BICD2):c.2544G>A (p.Glu848=) rs533026038 0.00014
NM_001003800.2(BICD2):c.1453G>T (p.Val485Phe) rs199519253 0.00013
NM_001003800.2(BICD2):c.1680C>T (p.Gly560=) rs371748461 0.00011
NM_001003800.2(BICD2):c.1401C>T (p.His467=) rs144442734 0.00009
NM_001003800.2(BICD2):c.1370G>A (p.Arg457His) rs370118099 0.00008
NM_001003800.2(BICD2):c.2350A>G (p.Met784Val) rs149891938 0.00008
NM_001003800.2(BICD2):c.1738C>T (p.Arg580Trp) rs573861187 0.00007
NM_001003800.2(BICD2):c.2142G>C (p.Lys714Asn) rs777986224 0.00007
NM_001003800.2(BICD2):c.981G>A (p.Pro327=) rs200288349 0.00006
NM_001003800.2(BICD2):c.1481A>G (p.Gln494Arg) rs142985475 0.00005
NM_001003800.2(BICD2):c.1501C>T (p.Arg501Trp) rs373224610 0.00005
NM_001003800.2(BICD2):c.1421A>G (p.Tyr474Cys) rs1014182946 0.00004
NM_001003800.2(BICD2):c.2469C>T (p.Ser823=) rs199989045 0.00004
NM_001003800.2(BICD2):c.2515G>A (p.Gly839Arg) rs756910200 0.00004
NM_001003800.2(BICD2):c.2541C>T (p.Ser847=) rs775345022 0.00004
NM_001003800.2(BICD2):c.684T>G (p.Asp228Glu) rs762107122 0.00004
NM_001003800.2(BICD2):c.1079C>T (p.Ala360Val) rs587777884 0.00003
NM_001003800.2(BICD2):c.1094C>T (p.Thr365Met) rs374704553 0.00003
NM_001003800.2(BICD2):c.1534G>A (p.Val512Ile) rs748921807 0.00002
NM_001003800.2(BICD2):c.1376C>T (p.Thr459Met) rs777065935 0.00001
NM_001003800.2(BICD2):c.1290C>T (p.Asn430=)
NM_001003800.2(BICD2):c.1530C>T (p.Ser510=)
NM_001003800.2(BICD2):c.1536C>T (p.Val512=)
NM_001003800.2(BICD2):c.1739G>A (p.Arg580Gln) rs775229197
NM_001003800.2(BICD2):c.1993G>T (p.Val665Leu) rs587777885
NM_001003800.2(BICD2):c.2058G>A (p.Lys686=)
NM_001003800.2(BICD2):c.2106+14C>T
NM_001003800.2(BICD2):c.2258+17C>T rs554612134
NM_001003800.2(BICD2):c.2258+18G>A rs376177099
NM_001003800.2(BICD2):c.2313T>A (p.Ala771=)
NM_001003800.2(BICD2):c.2497G>A (p.Asp833Asn)
NM_001003800.2(BICD2):c.453+9G>T rs202189685

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