ClinVar Miner

List of variants in gene LMX1B reported as benign for nail-patella syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_001174147.2(LMX1B):c.*2393T>C rs10120414 0.90738
NM_001174147.2(LMX1B):c.*2184A>G rs10733682 0.55594
NM_001174147.2(LMX1B):c.441A>G (p.Glu147=) rs2277158 0.45698
NM_001174147.2(LMX1B):c.*2394G>C rs10760451 0.44883
NM_001174147.2(LMX1B):c.*4171T>C rs3814119 0.44770
NM_001174147.2(LMX1B):c.*3864T>C rs10987419 0.42825
NM_001174147.2(LMX1B):c.*3833A>G rs10987418 0.42749
NM_001174147.2(LMX1B):c.*3771G>T rs10987417 0.41745
NM_001174147.2(LMX1B):c.726G>C (p.Ser242=) rs13295990 0.41484
NM_001174147.2(LMX1B):c.*3957C>A rs10987422 0.41441
NM_001174147.2(LMX1B):c.*1582A>G rs10987415 0.39164
NM_001174147.2(LMX1B):c.326+7G>C rs1336980 0.28269
NM_001174147.2(LMX1B):c.*1389T>G rs13300385 0.28012
NM_001174147.2(LMX1B):c.*3182A>G rs3861878 0.27278
NM_001174147.2(LMX1B):c.*2984C>T rs4083644 0.26400
NM_001174147.2(LMX1B):c.*3342T>C rs4083645 0.25994
NM_001174147.2(LMX1B):c.*748C>T rs10987414 0.25765
NM_001174147.2(LMX1B):c.*584C>T rs34200683 0.24353
NM_001174147.2(LMX1B):c.*1666C>T rs10987416 0.23942
NM_001174147.2(LMX1B):c.*708G>A rs10987413 0.22906
NM_001174147.2(LMX1B):c.*3346G>A rs7023938 0.21957
NM_001174147.2(LMX1B):c.*1255A>G rs16929236 0.18589
NM_001174147.2(LMX1B):c.*932G>T rs28687510 0.18581
NM_001174147.2(LMX1B):c.*1992T>C rs34776870 0.15317
NM_001174147.2(LMX1B):c.*1997G>A rs35632228 0.15118
NM_001174147.2(LMX1B):c.*898C>T rs10760450 0.14051
NM_001174147.2(LMX1B):c.*1393G>T rs13299451 0.12409
NM_001174147.2(LMX1B):c.*1473G>A rs13299609 0.11304
NM_001174147.2(LMX1B):c.*451C>T rs71497630 0.10571
NM_001174147.2(LMX1B):c.*51A>G rs10121481 0.08863
NM_001174147.2(LMX1B):c.*3881G>T rs10987421 0.08782
NM_001174147.2(LMX1B):c.*3865G>A rs10987420 0.08771
NM_001174147.2(LMX1B):c.*79G>A rs10115393 0.07595
NM_001174147.2(LMX1B):c.*27G>A rs10115373 0.06554
NM_001174147.2(LMX1B):c.*1304G>A rs73596779 0.06258
NM_001174147.2(LMX1B):c.*1716A>G rs116411474 0.02725
NM_001174147.2(LMX1B):c.930G>A (p.Thr310=) rs112171815 0.01716
NM_001174147.2(LMX1B):c.*2345G>A rs74429080 0.01611
NM_001174147.2(LMX1B):c.*127C>T rs113846301 0.01560
NM_001174147.2(LMX1B):c.*1574G>T rs148173186 0.01517
NM_001174147.2(LMX1B):c.*1995C>G rs74498940 0.01310
NM_001174147.2(LMX1B):c.*515A>G rs112375232 0.01060
NM_001174147.2(LMX1B):c.*280G>A rs111648919 0.01052
NM_001174147.2(LMX1B):c.*1644C>G rs187256465 0.01022
NM_001174147.2(LMX1B):c.*1604A>G rs146126278 0.00995
NM_001174147.2(LMX1B):c.*4373A>G rs78565800 0.00792
NM_001174147.2(LMX1B):c.*1538C>G rs144857145 0.00770
NM_001174147.2(LMX1B):c.*173G>A rs181701033 0.00529
NM_001174147.2(LMX1B):c.*4288G>A rs150407176 0.00469
NM_001174147.2(LMX1B):c.*3716C>G rs147614955 0.00324
NM_001174147.2(LMX1B):c.*884G>A rs146268507 0.00255
NM_001174147.2(LMX1B):c.*438G>C rs140325479 0.00095
NM_001174147.2(LMX1B):c.140-4A>G rs368126014 0.00047
NM_001174147.2(LMX1B):c.*4012C>T rs576424682 0.00046
NM_001174147.2(LMX1B):c.1200C>T (p.Phe400=) rs372183654 0.00030
NM_001174147.2(LMX1B):c.*1063T>A rs551202501 0.00026
NM_001174147.2(LMX1B):c.*3338C>G rs565879113 0.00026
NM_001174147.2(LMX1B):c.*2966G>A rs191951894 0.00015
NM_001174147.2(LMX1B):c.*2160C>T rs145937520 0.00014
NM_001174147.2(LMX1B):c.*155G>A rs151191848 0.00007
NM_001174147.2(LMX1B):c.*1287A>T rs572241075 0.00004
NM_001174147.2(LMX1B):c.552C>T (p.Ser184=) rs142488434 0.00003
NM_001174147.2(LMX1B):c.432C>T (p.Cys144=) rs375657880 0.00001
NM_001174147.2(LMX1B):c.*1673C>G rs191584459
NM_001174147.2(LMX1B):c.*1703C>T rs144070517
NM_001174147.2(LMX1B):c.*172C>A rs574095852
NM_001174147.2(LMX1B):c.*2590_*2591del rs398069012
NM_001174147.2(LMX1B):c.*2831C>T rs148906444
NM_001174147.2(LMX1B):c.*4127C>T rs146636393
NM_001174147.2(LMX1B):c.1107C>T (p.Ser369=) rs10115304
NM_001174147.2(LMX1B):c.628G>A (p.Gly210Arg) rs754095270

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