ClinVar Miner

List of variants in gene LAMB2 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP
NM_002292.3(LAMB2):c.*92A>G rs886058670
NM_002292.3(LAMB2):c.-112A>T rs546461860
NM_002292.3(LAMB2):c.-146G>T rs886058678
NM_002292.3(LAMB2):c.-200C>T rs886058679
NM_002292.3(LAMB2):c.-241T>C rs886058680
NM_002292.3(LAMB2):c.-252T>C rs886058681
NM_002292.3(LAMB2):c.-279A>T rs886058682
NM_002292.3(LAMB2):c.101C>A (p.Ala34Asp) rs202057459
NM_002292.3(LAMB2):c.1206G>A (p.Arg402=) rs201999373
NM_002292.3(LAMB2):c.1357C>T (p.Arg453Cys) rs765252703
NM_002292.3(LAMB2):c.1358G>A (p.Arg453His) rs1428596182
NM_002292.3(LAMB2):c.1403G>A (p.Arg468Gln)
NM_002292.3(LAMB2):c.1423C>T (p.Arg475Trp) rs144487632
NM_002292.3(LAMB2):c.1442G>A (p.Ser481Asn) rs144230655
NM_002292.3(LAMB2):c.149C>T (p.Ala50Val)
NM_002292.3(LAMB2):c.1682G>A (p.Arg561Gln) rs866448113
NM_002292.3(LAMB2):c.1750C>A (p.Arg584Ser)
NM_002292.3(LAMB2):c.1831C>T (p.Leu611=) rs886058676
NM_002292.3(LAMB2):c.1851G>A (p.Lys617=)
NM_002292.3(LAMB2):c.1931G>A (p.Arg644His)
NM_002292.3(LAMB2):c.2154G>A (p.Leu718=) rs886058675
NM_002292.3(LAMB2):c.2236C>T (p.Arg746Cys) rs200658738
NM_002292.3(LAMB2):c.2263G>C (p.Val755Leu)
NM_002292.3(LAMB2):c.2271C>A (p.Ser757Arg)
NM_002292.3(LAMB2):c.2295C>T (p.Cys765=) rs201289156
NM_002292.3(LAMB2):c.2297C>T (p.Ala766Val)
NM_002292.3(LAMB2):c.2322C>G (p.Thr774=) rs142116851
NM_002292.3(LAMB2):c.2434C>T (p.Arg812Cys) rs151134957
NM_002292.3(LAMB2):c.2435G>A (p.Arg812His) rs886058674
NM_002292.3(LAMB2):c.2459A>T (p.Tyr820Phe) rs746761674
NM_002292.3(LAMB2):c.250-14C>T rs371403310
NM_002292.3(LAMB2):c.253G>A (p.Glu85Lys) rs140371771
NM_002292.3(LAMB2):c.2720+13C>A rs369359244
NM_002292.3(LAMB2):c.2726T>C (p.Ile909Thr) rs201756319
NM_002292.3(LAMB2):c.280C>T (p.Arg94Trp) rs754551568
NM_002292.3(LAMB2):c.2810G>A (p.Arg937Gln) rs201235061
NM_002292.3(LAMB2):c.284G>A (p.Arg95His)
NM_002292.3(LAMB2):c.284G>C (p.Arg95Pro) rs147691227
NM_002292.3(LAMB2):c.2884+15delG rs769133638
NM_002292.3(LAMB2):c.2922G>C (p.Gly974=) rs145465720
NM_002292.3(LAMB2):c.2945G>A (p.Arg982Gln)
NM_002292.3(LAMB2):c.3036C>T (p.His1012=) rs777538430
NM_002292.3(LAMB2):c.3059C>A (p.Ala1020Asp)
NM_002292.3(LAMB2):c.3071C>T (p.Pro1024Leu) rs368506627
NM_002292.3(LAMB2):c.3109C>T (p.Arg1037Cys) rs201159870
NM_002292.3(LAMB2):c.3115A>C (p.Thr1039Pro) rs747604203
NM_002292.3(LAMB2):c.3192G>C (p.Gln1064His) rs1553778039
NM_002292.3(LAMB2):c.3198A>G (p.Pro1066=) rs886058673
NM_002292.3(LAMB2):c.3232C>T (p.Arg1078Cys) rs143284092
NM_002292.3(LAMB2):c.3325G>A (p.Glu1109Lys) rs79677861
NM_002292.3(LAMB2):c.3355G>A (p.Gly1119Ser) rs199570781
NM_002292.3(LAMB2):c.3547A>G (p.Ile1183Val) rs370877359
NM_002292.3(LAMB2):c.3582C>T (p.Phe1194=) rs138540017
NM_002292.3(LAMB2):c.3640C>T (p.Arg1214Trp)
NM_002292.3(LAMB2):c.3644C>G (p.Ala1215Gly) rs140456179
NM_002292.3(LAMB2):c.3664G>C (p.Gly1222Arg) rs748563846
NM_002292.3(LAMB2):c.3757G>A (p.Ala1253Thr) rs141062242
NM_002292.3(LAMB2):c.3763A>G (p.Thr1255Ala) rs1180166011
NM_002292.3(LAMB2):c.3797+5G>A rs150213016
NM_002292.3(LAMB2):c.386-15C>T rs117575041
NM_002292.3(LAMB2):c.4007C>T (p.Ala1336Val) rs886058672
NM_002292.3(LAMB2):c.4011T>C (p.His1337=) rs886058671
NM_002292.3(LAMB2):c.4034G>A (p.Arg1345His) rs75073433
NM_002292.3(LAMB2):c.4043A>G (p.Asn1348Ser) rs771215576
NM_002292.3(LAMB2):c.4118A>G (p.Asp1373Gly) rs112933248
NM_002292.3(LAMB2):c.4134C>T (p.Asp1378=) rs774234171
NM_002292.3(LAMB2):c.4140C>A (p.Asn1380Lys) rs267607207
NM_002292.3(LAMB2):c.4222C>T (p.Leu1408=) rs143974640
NM_002292.3(LAMB2):c.4274G>C (p.Gly1425Ala)
NM_002292.3(LAMB2):c.4304C>T (p.Pro1435Leu)
NM_002292.3(LAMB2):c.4369C>T (p.Arg1457Trp) rs151037751
NM_002292.3(LAMB2):c.4489A>G (p.Lys1497Glu) rs771769006
NM_002292.3(LAMB2):c.4559A>G (p.Lys1520Arg) rs148069401
NM_002292.3(LAMB2):c.4645G>T (p.Ala1549Ser) rs764494090
NM_002292.3(LAMB2):c.467G>A (p.Arg156His) rs1378409559
NM_002292.3(LAMB2):c.4751A>G (p.Glu1584Gly) rs768491835
NM_002292.3(LAMB2):c.4877G>C (p.Arg1626Pro) rs752674803
NM_002292.3(LAMB2):c.4878G>A (p.Arg1626=) rs148648480
NM_002292.3(LAMB2):c.4958T>C (p.Leu1653Pro) rs200761921
NM_002292.3(LAMB2):c.5021G>A (p.Arg1674Gln) rs764128779
NM_002292.3(LAMB2):c.5026G>A (p.Gly1676Arg) rs200747448
NM_002292.3(LAMB2):c.5027G>T (p.Gly1676Val) rs199580679
NM_002292.3(LAMB2):c.5039C>T (p.Ala1680Val) rs141473691
NM_002292.3(LAMB2):c.5109C>T (p.Arg1703=) rs151292828
NM_002292.3(LAMB2):c.5155C>T (p.Arg1719Cys) rs201458234
NM_002292.3(LAMB2):c.5213C>T (p.Ala1738Val) rs139156815
NM_002292.3(LAMB2):c.5240A>G (p.Asp1747Gly) rs777643155
NM_002292.3(LAMB2):c.527G>A (p.Arg176Gln)
NM_002292.3(LAMB2):c.5286T>C (p.Asn1762=) rs781092208
NM_002292.3(LAMB2):c.5379C>G (p.Ile1793Met) rs11550620
NM_002292.3(LAMB2):c.646G>A (p.Glu216Lys)
NM_002292.3(LAMB2):c.661G>A (p.Val221Met)
NM_002292.3(LAMB2):c.713-3C>T rs775876911
NM_002292.3(LAMB2):c.740T>C (p.Val247Ala) rs747693090
NM_002292.3(LAMB2):c.816T>C (p.Tyr272=) rs151251039
NM_002292.3(LAMB2):c.8T>C (p.Leu3Pro) rs373955878
NM_002292.3(LAMB2):c.916-4A>G rs886058677
NM_002292.3(LAMB2):c.922G>A (p.Gly308Arg) rs774169261
NM_002292.3(LAMB2):c.991C>T (p.Leu331=) rs561241970
NM_002292.4(LAMB2):c.511A>C (p.Thr171Pro)

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