ClinVar Miner

List of variants in gene LIM2 reported as uncertain significance for cataract

Included ClinVar conditions (65):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_001161748.2(LIM2):c.231C>T (p.Ser77=) rs8111243 0.01252
NM_001161748.2(LIM2):c.57G>A (p.Leu19=) rs142517355 0.00068
NM_001161748.2(LIM2):c.175+77T>C rs145192236 0.00063
NM_001161748.2(LIM2):c.502C>T (p.Arg168Cys) rs150085001 0.00056
NM_001161748.2(LIM2):c.175+50G>A rs147625714 0.00029
NM_001161748.2(LIM2):c.380T>C (p.Leu127Pro) rs142111893 0.00019
NM_001161748.2(LIM2):c.281G>A (p.Arg94His) rs770425768 0.00018
NM_001161748.2(LIM2):c.334G>A (p.Val112Ile) rs142030761 0.00014
NM_001161748.2(LIM2):c.131G>A (p.Arg44Gln) rs142234866 0.00011
NM_001161748.2(LIM2):c.193C>T (p.Arg65Trp) rs139154341 0.00008
NM_001161748.2(LIM2):c.*245A>G rs758862764 0.00007
NM_001161748.2(LIM2):c.108C>T (p.Ser36=) rs760441995 0.00006
NM_001161748.2(LIM2):c.175+113G>C rs754470902 0.00005
NM_001161748.2(LIM2):c.40G>A (p.Val14Met) rs202081431 0.00005
NM_001161748.2(LIM2):c.248T>C (p.Ile83Thr) rs773568535 0.00004
NM_001161748.2(LIM2):c.175+28G>A rs199913969 0.00003
NM_001161748.2(LIM2):c.484C>T (p.Arg162Trp) rs558484735 0.00003
NM_001161748.2(LIM2):c.-41G>A rs539594698 0.00002
NM_001161748.2(LIM2):c.24C>T (p.Gly8=) rs147551022 0.00002
NM_001161748.2(LIM2):c.*291T>C rs932195033 0.00001
NM_001161748.2(LIM2):c.-7+14G>A rs568064524 0.00001
NM_001161748.2(LIM2):c.174C>T (p.Ile58=) rs776429566 0.00001
NM_001161748.2(LIM2):c.175+30G>A rs376861251 0.00001
NM_001161748.2(LIM2):c.175+56C>T rs560748825 0.00001
NM_001161748.2(LIM2):c.175+87A>G rs369343996 0.00001
NM_001161748.2(LIM2):c.333C>T (p.Phe111=) rs566729340 0.00001
NM_001161748.2(LIM2):c.357C>T (p.Tyr119=) rs761154589 0.00001
NM_001161748.2(LIM2):c.500G>A (p.Arg167Gln) rs191407731 0.00001
NM_001161748.2(LIM2):c.*218C>G rs886054600
NM_001161748.2(LIM2):c.*58G>A rs569373539
NM_001161748.2(LIM2):c.-27C>A rs113926789
NM_001161748.2(LIM2):c.-29C>G rs886054601
NM_001161748.2(LIM2):c.100T>A (p.Ser34Thr) rs76269472
NM_001161748.2(LIM2):c.141G>C (p.Leu47=) rs1987093521
NM_001161748.2(LIM2):c.175+46G>A rs1987086753
NM_001161748.2(LIM2):c.321del (p.Ser108fs) rs1986917705
NM_001161748.2(LIM2):c.337G>A (p.Val113Met) rs73934370
NM_001161748.2(LIM2):c.337G>C (p.Val113Leu) rs73934370
NM_001161748.2(LIM2):c.356A>G (p.Tyr119Cys)
NM_001161748.2(LIM2):c.420C>A (p.Tyr140Ter) rs1212925287
NM_001161748.2(LIM2):c.440T>C (p.Val147Ala)
NM_001161748.2(LIM2):c.457G>A (p.Ala153Thr)
NM_001161748.2(LIM2):c.460+9G>A rs1568480003
NM_001161748.2(LIM2):c.487G>A (p.Val163Met)

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