ClinVar Miner

List of variants in gene LMX1B reported as uncertain significance for bone development disease

Included ClinVar conditions (614):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 125
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001174147.2(LMX1B):c.886+18C>T rs529668402 0.00104
NM_001174147.2(LMX1B):c.*950G>C rs568763153 0.00080
NM_001174147.2(LMX1B):c.*3731G>C rs566004764 0.00063
NM_001174147.2(LMX1B):c.*4206G>A rs762728003 0.00059
NM_001174147.2(LMX1B):c.*1754C>T rs886063434 0.00050
NM_001174147.2(LMX1B):c.*128G>A rs540930895 0.00045
NM_001174147.2(LMX1B):c.*3891G>A rs534775990 0.00044
NM_001174147.2(LMX1B):c.*3235C>T rs908803074 0.00031
NM_001174147.2(LMX1B):c.*3719G>A rs765341524 0.00028
NM_001174147.2(LMX1B):c.*355G>T rs886063422 0.00024
NM_001174147.2(LMX1B):c.*4129C>T rs148294658 0.00024
NM_001174147.2(LMX1B):c.*2023C>T rs574903734 0.00016
NM_001174147.2(LMX1B):c.*4123C>T rs906873628 0.00016
NM_001174147.2(LMX1B):c.*574C>T rs765510482 0.00016
NM_001174147.2(LMX1B):c.*3713G>A rs1015713642 0.00014
NM_001174147.2(LMX1B):c.*547C>T rs886063423 0.00014
NM_001174147.2(LMX1B):c.886+8G>A rs774459476 0.00012
NM_001174147.2(LMX1B):c.*446G>T rs894019334 0.00011
NM_001174147.2(LMX1B):c.*551C>A rs762152428 0.00011
NM_001174147.2(LMX1B):c.*4477C>T rs778454522 0.00010
NM_001174147.2(LMX1B):c.*1511G>A rs547510293 0.00009
NM_001174147.2(LMX1B):c.*90C>T rs747815548 0.00009
NM_001174147.2(LMX1B):c.972G>C (p.Gln324His) rs886063418 0.00009
NM_001174147.2(LMX1B):c.*2511C>T rs868840331 0.00008
NM_001174147.2(LMX1B):c.*3804C>T rs558013035 0.00008
NM_001174147.2(LMX1B):c.*3404G>A rs754688626 0.00007
NM_001174147.2(LMX1B):c.*4050C>A rs776459298 0.00007
NM_001174147.2(LMX1B):c.130G>A (p.Val44Met) rs1017526258 0.00007
NM_001174147.2(LMX1B):c.*1676G>A rs886063431 0.00006
NM_001174147.2(LMX1B):c.*230C>T rs531744651 0.00006
NM_001174147.2(LMX1B):c.*2620G>A rs950531780 0.00006
NM_001174147.2(LMX1B):c.*3385C>A rs886063440 0.00006
NM_001174147.2(LMX1B):c.*4157C>T rs185290341 0.00006
NM_001174147.2(LMX1B):c.*18G>A rs755294493 0.00005
NM_001174147.2(LMX1B):c.*4466C>A rs918457009 0.00005
NM_001174147.2(LMX1B):c.*44G>T rs773048475 0.00005
NM_001174147.2(LMX1B):c.742-6A>T rs554576629 0.00005
NM_001174147.2(LMX1B):c.742-7G>C rs534963836 0.00005
NM_001174147.2(LMX1B):c.*1266T>G rs558658509 0.00004
NM_001174147.2(LMX1B):c.*3464G>A rs920113788 0.00004
NM_001174147.2(LMX1B):c.*3765A>C rs886063444 0.00004
NM_001174147.2(LMX1B):c.*681C>T rs138360048 0.00004
NM_001174147.2(LMX1B):c.349G>A (p.Gly117Ser) rs773332016 0.00004
NM_001174147.2(LMX1B):c.375C>T (p.Thr125=) rs921576454 0.00004
NM_001174147.2(LMX1B):c.463G>A (p.Glu155Lys) rs776839118 0.00004
NM_001174147.2(LMX1B):c.*3098A>G rs749654121 0.00003
NM_001174147.2(LMX1B):c.*3805G>A rs886063445 0.00003
NM_001174147.2(LMX1B):c.958G>A (p.Val320Met) rs778847250 0.00003
NM_001174147.2(LMX1B):c.*1189C>T rs918993617 0.00002
NM_001174147.2(LMX1B):c.*232C>T rs551852198 0.00002
NM_001174147.2(LMX1B):c.*2737C>T rs767564570 0.00002
NM_001174147.2(LMX1B):c.*317G>A rs1298736368 0.00002
NM_001174147.2(LMX1B):c.*3522G>A rs886063442 0.00002
NM_001174147.2(LMX1B):c.*4128G>A rs886063447 0.00002
NM_001174147.2(LMX1B):c.*553C>T rs1279736588 0.00002
NM_001174147.2(LMX1B):c.*635A>G rs1443082300 0.00002
NM_001174147.2(LMX1B):c.*999C>G rs919370292 0.00002
NM_001174147.2(LMX1B):c.1151G>A (p.Arg384His) rs143906016 0.00002
NM_001174147.2(LMX1B):c.508G>A (p.Glu170Lys) rs199738980 0.00002
NM_001174147.2(LMX1B):c.57G>A (p.Thr19=) rs376265443 0.00002
NM_001174147.2(LMX1B):c.742-15C>G rs566334716 0.00002
NM_001174147.2(LMX1B):c.*1493C>T rs908912434 0.00001
NM_001174147.2(LMX1B):c.*1713C>T rs886063432 0.00001
NM_001174147.2(LMX1B):c.*1899G>A rs756806649 0.00001
NM_001174147.2(LMX1B):c.*286C>T rs1050105993 0.00001
NM_001174147.2(LMX1B):c.*3196G>A rs1386261176 0.00001
NM_001174147.2(LMX1B):c.*3379C>T rs886063439 0.00001
NM_001174147.2(LMX1B):c.*3642G>T rs886063443 0.00001
NM_001174147.2(LMX1B):c.*401G>A rs548738973 0.00001
NM_001174147.2(LMX1B):c.*4338G>C rs1035726771 0.00001
NM_001174147.2(LMX1B):c.*4570A>G rs886063449 0.00001
NM_001174147.2(LMX1B):c.-12G>T rs563572406 0.00001
NM_001174147.2(LMX1B):c.115C>T (p.Pro39Ser) rs771784052 0.00001
NM_001174147.2(LMX1B):c.1201G>A (p.Ala401Thr) rs761796969 0.00001
NM_001174147.2(LMX1B):c.520G>A (p.Asp174Asn) rs1766593692 0.00001
NM_001174147.2(LMX1B):c.559G>A (p.Val187Met) rs765969991 0.00001
NM_001174147.2(LMX1B):c.637G>A (p.Gly213Arg) rs1472509996 0.00001
NM_001174147.2(LMX1B):c.720C>T (p.Val240=) rs1203103557 0.00001
NM_001174147.2(LMX1B):c.*105C>G rs953659561
NM_001174147.2(LMX1B):c.*1115T>A rs886063425
NM_001174147.2(LMX1B):c.*1164A>T rs2030387692
NM_001174147.2(LMX1B):c.*1387TGTTT[10] rs59836255
NM_001174147.2(LMX1B):c.*1387TGTTT[12] rs59836255
NM_001174147.2(LMX1B):c.*1387TGTTT[8] rs59836255
NM_001174147.2(LMX1B):c.*1389_*1398delinsGTTTT rs886063427
NM_001174147.2(LMX1B):c.*1389_*1408delinsGTTTT rs886063428
NM_001174147.2(LMX1B):c.*1531T>G rs886063429
NM_001174147.2(LMX1B):c.*1542A>G rs886063430
NM_001174147.2(LMX1B):c.*1612C>T rs767599284
NM_001174147.2(LMX1B):c.*1737T>C rs886063433
NM_001174147.2(LMX1B):c.*17C>T rs754093597
NM_001174147.2(LMX1B):c.*1935G>A rs886063435
NM_001174147.2(LMX1B):c.*2062C>A rs1453922739
NM_001174147.2(LMX1B):c.*2344C>T rs983206651
NM_001174147.2(LMX1B):c.*2456CTT[1] rs886063436
NM_001174147.2(LMX1B):c.*253C>T rs748844195
NM_001174147.2(LMX1B):c.*2612T>C rs886063437
NM_001174147.2(LMX1B):c.*277C>T rs886063421
NM_001174147.2(LMX1B):c.*3021T>G rs886063438
NM_001174147.2(LMX1B):c.*3052T>C rs2030467754
NM_001174147.2(LMX1B):c.*3274T>G rs539927124
NM_001174147.2(LMX1B):c.*3335A>G rs2030478207
NM_001174147.2(LMX1B):c.*3346G>T rs7023938
NM_001174147.2(LMX1B):c.*3400G>A rs886063441
NM_001174147.2(LMX1B):c.*3403C>G rs776860982
NM_001174147.2(LMX1B):c.*3799G>T rs2030493794
NM_001174147.2(LMX1B):c.*3908T>C rs886063446
NM_001174147.2(LMX1B):c.*4303T>C rs545179114
NM_001174147.2(LMX1B):c.*4303T>G rs545179114
NM_001174147.2(LMX1B):c.*4331T>C rs886063448
NM_001174147.2(LMX1B):c.*4568C>A rs539011309
NM_001174147.2(LMX1B):c.*575G>T rs549542139
NM_001174147.2(LMX1B):c.*59C>T rs886063420
NM_001174147.2(LMX1B):c.*745G>A rs2030369522
NM_001174147.2(LMX1B):c.*764A>C rs897459902
NM_001174147.2(LMX1B):c.1052-5C>A rs886063419
NM_001174147.2(LMX1B):c.139+5G>C rs1114167421
NM_001174147.2(LMX1B):c.237G>T (p.Glu79Asp) rs2118823518
NM_001174147.2(LMX1B):c.253G>A (p.Ala85Thr) rs1289892661
NM_001174147.2(LMX1B):c.451C>T (p.Arg151Cys) rs149434820
NM_001174147.2(LMX1B):c.628G>C (p.Gly210Arg) rs754095270
NM_001174147.2(LMX1B):c.647C>T (p.Pro216Leu) rs779417752
NM_001174147.2(LMX1B):c.820-13G>A rs914683099
NM_001174147.2(LMX1B):c.886+36G>A
NM_001174147.2(LMX1B):c.94G>A (p.Glu32Lys) rs748676035

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.