ClinVar Miner

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

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_002316.3(LMX1B):c.*1255A>G rs16929236
NM_002316.3(LMX1B):c.*1304G>A rs73596779
NM_002316.3(LMX1B):c.*1389T>G rs13300385
NM_002316.3(LMX1B):c.*1393G>T rs13299451
NM_002316.3(LMX1B):c.*1473G>A rs13299609
NM_002316.3(LMX1B):c.*1582A>G rs10987415
NM_002316.3(LMX1B):c.*1666C>T rs10987416
NM_002316.3(LMX1B):c.*1992T>C rs34776870
NM_002316.3(LMX1B):c.*1997G>A rs35632228
NM_002316.3(LMX1B):c.*2184A>G rs10733682
NM_002316.3(LMX1B):c.*2393T>C rs10120414
NM_002316.3(LMX1B):c.*2394G>C rs10760451
NM_002316.3(LMX1B):c.*2590_*2591del rs398069012
NM_002316.3(LMX1B):c.*27G>A rs10115373
NM_002316.3(LMX1B):c.*2984C>T rs4083644
NM_002316.3(LMX1B):c.*3182A>G rs3861878
NM_002316.3(LMX1B):c.*3342T>C rs4083645
NM_002316.3(LMX1B):c.*3346G>A rs7023938
NM_002316.3(LMX1B):c.*3771G>T rs10987417
NM_002316.3(LMX1B):c.*3833A>G rs10987418
NM_002316.3(LMX1B):c.*3864T>C rs10987419
NM_002316.3(LMX1B):c.*3881G>T rs10987421
NM_002316.3(LMX1B):c.*3957C>A rs10987422
NM_002316.3(LMX1B):c.*4171T>C rs3814119
NM_002316.3(LMX1B):c.*451C>T rs71497630
NM_002316.3(LMX1B):c.*51A>G rs10121481
NM_002316.3(LMX1B):c.*584C>T rs34200683
NM_002316.3(LMX1B):c.*708G>A rs10987413
NM_002316.3(LMX1B):c.*748C>T rs10987414
NM_002316.3(LMX1B):c.*79G>A rs10115393
NM_002316.3(LMX1B):c.*898C>T rs10760450
NM_002316.3(LMX1B):c.*932G>T rs28687510
NM_002316.3(LMX1B):c.1086C>T (p.Ser362=) rs10115304
NM_002316.3(LMX1B):c.326+7G>C rs1336980
NM_002316.3(LMX1B):c.441A>G (p.Glu147=) rs2277158
NM_002316.3(LMX1B):c.726G>C (p.Ser242=) rs13295990

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