ClinVar Miner

List of variants reported as uncertain significance for Majeed syndrome by Invitae

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 66
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HGVS dbSNP
NC_000018.9:g.(?_2920271)_(2960858_?)dup
NM_001375808.1(LPIN2):c.616_618GAA[2] (p.Glu208del)
NM_014646.2(LPIN2):c.106G>A (p.Val36Ile) rs774019375
NM_014646.2(LPIN2):c.1082C>T (p.Ala361Val) rs767142433
NM_014646.2(LPIN2):c.1099G>A (p.Ala367Thr) rs540544894
NM_014646.2(LPIN2):c.1118C>T (p.Pro373Leu)
NM_014646.2(LPIN2):c.1132C>T (p.Pro378Ser) rs201678207
NM_014646.2(LPIN2):c.1133C>T (p.Pro378Leu) rs146067222
NM_014646.2(LPIN2):c.1151C>T (p.Ser384Leu) rs765616457
NM_014646.2(LPIN2):c.1154C>T (p.Pro385Leu) rs754221410
NM_014646.2(LPIN2):c.1168+4A>G rs368340969
NM_014646.2(LPIN2):c.1168+6C>T rs200130790
NM_014646.2(LPIN2):c.1169-3C>T rs200259086
NM_014646.2(LPIN2):c.1169G>C (p.Gly390Ala)
NM_014646.2(LPIN2):c.1199C>T (p.Pro400Leu)
NM_014646.2(LPIN2):c.1203T>G (p.Asp401Glu) rs1018736752
NM_014646.2(LPIN2):c.1282G>A (p.Gly428Ser) rs768189312
NM_014646.2(LPIN2):c.1312C>T (p.Leu438Phe) rs138079183
NM_014646.2(LPIN2):c.1315T>C (p.Ser439Pro) rs1555673672
NM_014646.2(LPIN2):c.131A>G (p.Gln44Arg)
NM_014646.2(LPIN2):c.1322C>G (p.Ser441Cys)
NM_014646.2(LPIN2):c.1339G>A (p.Val447Met) rs373758040
NM_014646.2(LPIN2):c.1367C>T (p.Thr456Ile) rs368807055
NM_014646.2(LPIN2):c.1514T>C (p.Ile505Thr) rs146424724
NM_014646.2(LPIN2):c.1522C>T (p.Pro508Ser) rs1598528577
NM_014646.2(LPIN2):c.1711C>T (p.Leu571=)
NM_014646.2(LPIN2):c.1796C>T (p.Pro599Leu) rs372850864
NM_014646.2(LPIN2):c.1938+4A>G rs1397526157
NM_014646.2(LPIN2):c.1939-5A>G rs779830291
NM_014646.2(LPIN2):c.1957G>A (p.Asp653Asn)
NM_014646.2(LPIN2):c.1975G>A (p.Val659Met)
NM_014646.2(LPIN2):c.200T>C (p.Ile67Thr) rs1385257235
NM_014646.2(LPIN2):c.2088G>A (p.Lys696=) rs778440902
NM_014646.2(LPIN2):c.2091G>A (p.Ser697=)
NM_014646.2(LPIN2):c.2171A>G (p.Asn724Ser) rs140915714
NM_014646.2(LPIN2):c.2224G>A (p.Asp742Asn) rs779538504
NM_014646.2(LPIN2):c.2237G>A (p.Gly746Asp) rs1555672260
NM_014646.2(LPIN2):c.2261A>G (p.Lys754Arg)
NM_014646.2(LPIN2):c.2279G>A (p.Arg760Gln)
NM_014646.2(LPIN2):c.2409G>C (p.Gln803His) rs876660987
NM_014646.2(LPIN2):c.2420C>T (p.Ala807Val) rs752533626
NM_014646.2(LPIN2):c.2531A>G (p.Lys844Arg)
NM_014646.2(LPIN2):c.2569G>T (p.Val857Leu) rs1346809433
NM_014646.2(LPIN2):c.2617C>A (p.Pro873Thr) rs757315664
NM_014646.2(LPIN2):c.2621G>A (p.Cys874Tyr) rs201160155
NM_014646.2(LPIN2):c.2623C>A (p.Pro875Thr)
NM_014646.2(LPIN2):c.2650C>T (p.Arg884Ter) rs547662448
NM_014646.2(LPIN2):c.2657C>T (p.Pro886Leu) rs147203309
NM_014646.2(LPIN2):c.2671G>A (p.Asp891Asn) rs200648652
NM_014646.2(LPIN2):c.353T>C (p.Ile118Thr) rs181542503
NM_014646.2(LPIN2):c.374C>G (p.Ser125Trp) rs542116963
NM_014646.2(LPIN2):c.377G>A (p.Gly126Asp) rs778376881
NM_014646.2(LPIN2):c.388A>G (p.Thr130Ala) rs191101701
NM_014646.2(LPIN2):c.496A>G (p.Ser166Gly)
NM_014646.2(LPIN2):c.517G>A (p.Ala173Thr) rs140609636
NM_014646.2(LPIN2):c.523G>C (p.Ala175Pro) rs1334969199
NM_014646.2(LPIN2):c.584C>G (p.Ala195Gly) rs1226336598
NM_014646.2(LPIN2):c.584C>T (p.Ala195Val) rs1226336598
NM_014646.2(LPIN2):c.698C>T (p.Thr233Ile) rs139654849
NM_014646.2(LPIN2):c.71A>G (p.Gln24Arg) rs1568575278
NM_014646.2(LPIN2):c.755C>T (p.Ala252Val) rs774296727
NM_014646.2(LPIN2):c.802G>A (p.Gly268Arg) rs755432834
NM_014646.2(LPIN2):c.830A>G (p.Lys277Arg)
NM_014646.2(LPIN2):c.840A>G (p.Arg280=) rs780138552
NM_014646.2(LPIN2):c.907A>C (p.Ser303Arg) rs139798681
NM_014646.2(LPIN2):c.970A>T (p.Ile324Leu) rs1476358117

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