ClinVar Miner

List of variants in gene LMX1B reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP
NM_001174146.1(LMX1B):c.*1387_*1391TGTTT[10] rs59836255
NM_001174146.1(LMX1B):c.*1387_*1391TGTTT[12] rs59836255
NM_001174146.1(LMX1B):c.*1387_*1391TGTTT[8] rs59836255
NM_001174146.1(LMX1B):c.*2456_*2458CTT[1] rs886063436
NM_002316.3(LMX1B):c.*1115T>A rs886063425
NM_002316.3(LMX1B):c.*1266T>G rs558658509
NM_002316.3(LMX1B):c.*1389_*1398delinsGTTTT rs886063427
NM_002316.3(LMX1B):c.*1389_*1408delinsGTTTT rs886063428
NM_002316.3(LMX1B):c.*1511G>A rs547510293
NM_002316.3(LMX1B):c.*1531T>G rs886063429
NM_002316.3(LMX1B):c.*1542A>G rs886063430
NM_002316.3(LMX1B):c.*1612C>T rs767599284
NM_002316.3(LMX1B):c.*1676G>A rs886063431
NM_002316.3(LMX1B):c.*1713C>T rs886063432
NM_002316.3(LMX1B):c.*1737T>C rs886063433
NM_002316.3(LMX1B):c.*1754C>T rs886063434
NM_002316.3(LMX1B):c.*1935G>A rs886063435
NM_002316.3(LMX1B):c.*230C>T rs531744651
NM_002316.3(LMX1B):c.*232C>T rs551852198
NM_002316.3(LMX1B):c.*2612T>C rs886063437
NM_002316.3(LMX1B):c.*277C>T rs886063421
NM_002316.3(LMX1B):c.*3021T>G rs886063438
NM_002316.3(LMX1B):c.*3098A>G rs749654121
NM_002316.3(LMX1B):c.*3274T>G rs539927124
NM_002316.3(LMX1B):c.*3346G>T rs7023938
NM_002316.3(LMX1B):c.*3379C>T rs886063439
NM_002316.3(LMX1B):c.*3385C>A rs886063440
NM_002316.3(LMX1B):c.*3400G>A rs886063441
NM_002316.3(LMX1B):c.*3404G>A rs754688626
NM_002316.3(LMX1B):c.*3522G>A rs886063442
NM_002316.3(LMX1B):c.*355G>T rs886063422
NM_002316.3(LMX1B):c.*3642G>T rs886063443
NM_002316.3(LMX1B):c.*3765A>C rs886063444
NM_002316.3(LMX1B):c.*3805G>A rs886063445
NM_002316.3(LMX1B):c.*3908T>C rs886063446
NM_002316.3(LMX1B):c.*401G>A rs548738973
NM_002316.3(LMX1B):c.*4128G>A rs886063447
NM_002316.3(LMX1B):c.*4157C>T rs185290341
NM_002316.3(LMX1B):c.*4206G>A rs762728003
NM_002316.3(LMX1B):c.*4303T>C rs545179114
NM_002316.3(LMX1B):c.*4303T>G rs545179114
NM_002316.3(LMX1B):c.*4331T>C rs886063448
NM_002316.3(LMX1B):c.*4477C>T rs778454522
NM_002316.3(LMX1B):c.*4570A>G rs886063449
NM_002316.3(LMX1B):c.*547C>T rs886063423
NM_002316.3(LMX1B):c.*574C>T rs765510482
NM_002316.3(LMX1B):c.*59C>T rs886063420
NM_002316.3(LMX1B):c.1031-5C>A rs886063419
NM_002316.3(LMX1B):c.1130G>A (p.Arg377His)
NM_002316.3(LMX1B):c.1131C>T (p.Arg377=) rs146476348
NM_002316.3(LMX1B):c.139+5G>C rs1114167421
NM_002316.3(LMX1B):c.19C>G (p.Pro7Ala) rs767281663
NM_002316.3(LMX1B):c.381C>T (p.Phe127=) rs540034621
NM_002316.3(LMX1B):c.459C>T (p.Gly153=) rs779330478
NM_002316.3(LMX1B):c.57G>A (p.Thr19=) rs376265443
NM_002316.3(LMX1B):c.628G>A (p.Gly210Arg) rs754095270
NM_002316.3(LMX1B):c.628G>C (p.Gly210Arg) rs754095270
NM_002316.3(LMX1B):c.647C>T (p.Pro216Leu) rs779417752
NM_002316.3(LMX1B):c.741+14G>A rs527313096
NM_002316.3(LMX1B):c.742-15C>G rs566334716
NM_002316.3(LMX1B):c.742-6A>T rs554576629
NM_002316.3(LMX1B):c.742-7G>C rs534963836
NM_002316.3(LMX1B):c.972G>C (p.Gln324His) rs886063418

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