ClinVar Miner

List of variants in gene LPIN2 studied for Autoinflammatory syndrome

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Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_001375808.2(LPIN2):c.*3C>T rs3745012 0.27581
NM_001375808.2(LPIN2):c.*501T>C rs35176958 0.05733
NM_001375808.2(LPIN2):c.*99C>T rs143728428 0.01403
NM_001375808.2(LPIN2):c.2223C>T (p.Ala741=) rs17555442 0.01175
NM_001375808.2(LPIN2):c.1867C>T (p.Pro623Ser) rs143090653 0.00873
NM_001375808.2(LPIN2):c.1801G>A (p.Glu601Lys) rs61735393 0.00824
NM_001375808.2(LPIN2):c.147C>T (p.His49=) rs17886056 0.00707
NM_001375808.2(LPIN2):c.*358G>A rs184193388 0.00608
NM_001375808.2(LPIN2):c.590+6A>G rs73375280 0.00468
NM_001375808.2(LPIN2):c.1510C>T (p.Leu504Phe) rs104895500 0.00262
NM_001375808.2(LPIN2):c.120T>C (p.Asp40=) rs143261167 0.00243
NM_001375808.2(LPIN2):c.1735T>C (p.Ser579Pro) rs150022314 0.00221
NM_001375808.2(LPIN2):c.991G>T (p.Ala331Ser) rs80338805 0.00142
NM_001375808.2(LPIN2):c.1159A>G (p.Lys387Glu) rs104895501 0.00083
NM_001375808.2(LPIN2):c.1876C>T (p.Pro626Ser) rs150806357 0.00083
NM_001375808.2(LPIN2):c.1815G>A (p.Ser605=) rs143702044 0.00066
NM_001375808.2(LPIN2):c.2583C>T (p.Phe861=) rs141043192 0.00053
NM_001375808.2(LPIN2):c.1043C>T (p.Pro348Leu) rs34676691 0.00051
NM_001375808.2(LPIN2):c.2568C>T (p.Leu856=) rs149862905 0.00050
NM_001375808.2(LPIN2):c.517G>A (p.Ala173Thr) rs140609636 0.00048
NM_001375808.2(LPIN2):c.2443-9C>T rs191749331 0.00046
NM_001375808.2(LPIN2):c.446C>T (p.Pro149Leu) rs147615538 0.00037
NM_001375808.2(LPIN2):c.2671G>A (p.Asp891Asn) rs200648652 0.00033
NM_001375808.2(LPIN2):c.2625G>A (p.Pro875=) rs187572602 0.00027
NM_001375808.2(LPIN2):c.516C>T (p.Ala172=) rs150312425 0.00026
NM_001375808.2(LPIN2):c.2610C>T (p.Ser870=) rs145412418 0.00025
NM_001375808.2(LPIN2):c.1168+6C>T rs200130790 0.00024
NM_001375808.2(LPIN2):c.2445T>C (p.Asp815=) rs140249737 0.00021
NM_001375808.2(LPIN2):c.1489G>A (p.Glu497Lys) rs201325845 0.00013
NM_001375808.2(LPIN2):c.1783G>C (p.Ala595Pro) rs373929015 0.00013
NM_001375808.2(LPIN2):c.698C>T (p.Thr233Ile) rs139654849 0.00013
NM_001375808.2(LPIN2):c.1169-3C>T rs200259086 0.00011
NM_001375808.2(LPIN2):c.1888G>A (p.Gly630Ser) rs148607670 0.00011
NM_001375808.2(LPIN2):c.2371C>T (p.Leu791=) rs373520277 0.00011
NM_001375808.2(LPIN2):c.2535A>C (p.Gly845=) rs186864136 0.00011
NM_001375808.2(LPIN2):c.2657C>T (p.Pro886Leu) rs147203309 0.00011
NM_001375808.2(LPIN2):c.1134G>A (p.Pro378=) rs543890845 0.00009
NM_001375808.2(LPIN2):c.2658G>A (p.Pro886=) rs371358114 0.00009
NM_001375808.2(LPIN2):c.608C>T (p.Ser203Phe) rs144555528 0.00006
NM_001375808.2(LPIN2):c.*5G>A rs531230516 0.00005
NM_001375808.2(LPIN2):c.1282G>A (p.Gly428Ser) rs768189312 0.00004
NM_001375808.2(LPIN2):c.1435G>A (p.Glu479Lys) rs571085377 0.00003
NM_001375808.2(LPIN2):c.553G>A (p.Val185Met) rs148620026 0.00003
NM_001375808.2(LPIN2):c.858G>A (p.Arg286=) rs548077620 0.00003
NM_001375808.2(LPIN2):c.1122A>G (p.Ser374=) rs748347465 0.00002
NM_001375808.2(LPIN2):c.1347C>T (p.Ser449=) rs773074044 0.00002
NM_001375808.2(LPIN2):c.1204_1205dup (p.Asp402fs) rs779553737 0.00001
NM_001375808.2(LPIN2):c.1720T>A (p.Ser574Thr) rs148779863 0.00001
NM_001375808.2(LPIN2):c.1745C>T (p.Pro582Leu) rs755110304 0.00001
NM_001375808.2(LPIN2):c.1923C>T (p.Leu641=) rs183435741 0.00001
NM_001375808.2(LPIN2):c.2034G>C (p.Leu678=) rs749526038 0.00001
NM_001375808.2(LPIN2):c.2076G>C (p.Gly692=) rs781016213 0.00001
NM_001375808.2(LPIN2):c.2171A>G (p.Asn724Ser) rs140915714 0.00001
NM_001375808.2(LPIN2):c.2201C>T (p.Ser734Leu) rs80338807 0.00001
NM_001375808.2(LPIN2):c.2317G>A (p.Ala773Thr) rs750526323 0.00001
NM_001375808.2(LPIN2):c.2410C>A (p.Pro804Thr) rs1290776094 0.00001
NM_001375808.2(LPIN2):c.2463A>G (p.Gln821=) rs1295333459 0.00001
NM_001375808.2(LPIN2):c.2609C>G (p.Ser870Cys) rs769901079 0.00001
NM_001375808.2(LPIN2):c.2674C>T (p.Leu892=) rs1414200193 0.00001
NM_001375808.2(LPIN2):c.359C>A (p.Thr120Asn) rs562075898 0.00001
NM_001375808.2(LPIN2):c.54C>A (p.Leu18=) rs753729438 0.00001
NM_001375808.2(LPIN2):c.794C>T (p.Thr265Met) rs1334562388 0.00001
NM_001375808.2(LPIN2):c.907A>C (p.Ser303Arg) rs139798681 0.00001
NM_001375808.2(LPIN2):c.944C>T (p.Ala315Val) rs777659252 0.00001
NM_001375808.2(LPIN2):c.1169-7del rs746626720
NM_001375808.2(LPIN2):c.1265A>G (p.Lys422Arg) rs2144177505
NM_001375808.2(LPIN2):c.1428C>T (p.Gly476=) rs2077209708
NM_001375808.2(LPIN2):c.1442G>C (p.Gly481Ala) rs377661526
NM_001375808.2(LPIN2):c.1626A>C (p.Thr542=) rs1568519739
NM_001375808.2(LPIN2):c.1726G>A (p.Glu576Lys) rs946046520
NM_001375808.2(LPIN2):c.1756G>A (p.Asp586Asn) rs2144139779
NM_001375808.2(LPIN2):c.2011C>T (p.Arg671Cys) rs773597485
NM_001375808.2(LPIN2):c.220G>A (p.Val74Met) rs755936540
NM_001375808.2(LPIN2):c.2327+7C>T rs2144118376
NM_001375808.2(LPIN2):c.2451T>C (p.Tyr817=) rs2144112680
NM_001375808.2(LPIN2):c.2506G>A (p.Gly836Ser) rs2077042449
NM_001375808.2(LPIN2):c.2621G>T (p.Cys874Phe) rs201160155
NM_001375808.2(LPIN2):c.2628G>A (p.Glu876=) rs2144110086
NM_001375808.2(LPIN2):c.422T>C (p.Leu141Ser) rs763550824
NM_001375808.2(LPIN2):c.436A>G (p.Ile146Val) rs2143107101
NM_001375808.2(LPIN2):c.501G>C (p.Lys167Asn) rs751939691
NM_001375808.2(LPIN2):c.572A>G (p.Lys191Arg) rs778040063
NM_001375808.2(LPIN2):c.699-8C>G rs1568540842

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