ClinVar Miner

List of variants in gene LAMB2 reported as likely benign for Pierson syndrome; Nephrotic syndrome, type 5, with or without ocular abnormalities

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Total variants: 78
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HGVS dbSNP
NM_002292.4(LAMB2):c.1014C>T (p.Asp338=) rs150731491
NM_002292.4(LAMB2):c.109C>G (p.Pro37Ala) rs144765752
NM_002292.4(LAMB2):c.114T>C (p.Asp38=)
NM_002292.4(LAMB2):c.1206G>A (p.Arg402=) rs201999373
NM_002292.4(LAMB2):c.1218G>A (p.Val406=) rs1284533242
NM_002292.4(LAMB2):c.1306G>A (p.Gly436Ser) rs142402808
NM_002292.4(LAMB2):c.1311G>A (p.Gln437=) rs754837577
NM_002292.4(LAMB2):c.1391G>A (p.Arg464His) rs188487818
NM_002292.4(LAMB2):c.1405+9C>T
NM_002292.4(LAMB2):c.1422A>C (p.Ala474=) rs201408584
NM_002292.4(LAMB2):c.1446T>C (p.Thr482=) rs778631081
NM_002292.4(LAMB2):c.1519-6G>A
NM_002292.4(LAMB2):c.1542C>T (p.His514=) rs150783390
NM_002292.4(LAMB2):c.1551C>T (p.Leu517=)
NM_002292.4(LAMB2):c.1569C>T (p.Asp523=) rs1169038040
NM_002292.4(LAMB2):c.1572C>T (p.Cys524=) rs111883392
NM_002292.4(LAMB2):c.1614A>T (p.Thr538=)
NM_002292.4(LAMB2):c.1797C>T (p.Phe599=)
NM_002292.4(LAMB2):c.1890+9C>T rs1575535180
NM_002292.4(LAMB2):c.1891-10G>A rs746381319
NM_002292.4(LAMB2):c.189T>C (p.Thr63=) rs200171185
NM_002292.4(LAMB2):c.2018+8C>A rs1553778611
NM_002292.4(LAMB2):c.2019-8G>A rs377396194
NM_002292.4(LAMB2):c.2152-5T>C
NM_002292.4(LAMB2):c.216C>T (p.Gly72=) rs768806166
NM_002292.4(LAMB2):c.2322C>G (p.Thr774=) rs142116851
NM_002292.4(LAMB2):c.2373G>A (p.Leu791=) rs1478443594
NM_002292.4(LAMB2):c.2433C>T (p.Arg811=)
NM_002292.4(LAMB2):c.2475C>T (p.Pro825=) rs1575533579
NM_002292.4(LAMB2):c.2489-7C>T rs374958213
NM_002292.4(LAMB2):c.252C>T (p.Asp84=)
NM_002292.4(LAMB2):c.253G>A (p.Glu85Lys) rs140371771
NM_002292.4(LAMB2):c.2724C>T (p.Cys908=) rs142012138
NM_002292.4(LAMB2):c.2727T>C (p.Ile909=) rs376904255
NM_002292.4(LAMB2):c.2754G>T (p.Leu918=)
NM_002292.4(LAMB2):c.2885-8G>A rs374181186
NM_002292.4(LAMB2):c.2922G>C (p.Gly974=) rs145465720
NM_002292.4(LAMB2):c.2974A>G (p.Ile992Val)
NM_002292.4(LAMB2):c.2975T>C (p.Ile992Thr) rs148732023
NM_002292.4(LAMB2):c.3045G>A (p.Glu1015=) rs746638105
NM_002292.4(LAMB2):c.3141G>A (p.Pro1047=) rs373002075
NM_002292.4(LAMB2):c.3294C>T (p.His1098=) rs376981766
NM_002292.4(LAMB2):c.3327+8A>C rs756229789
NM_002292.4(LAMB2):c.3533G>A (p.Arg1178His)
NM_002292.4(LAMB2):c.3573T>C (p.His1191=) rs1343630379
NM_002292.4(LAMB2):c.3582C>T (p.Phe1194=) rs138540017
NM_002292.4(LAMB2):c.3756C>T (p.Ala1252=)
NM_002292.4(LAMB2):c.3797+4C>T
NM_002292.4(LAMB2):c.3875A>T (p.Asn1292Ile) rs148246465
NM_002292.4(LAMB2):c.4071T>C (p.Pro1357=)
NM_002292.4(LAMB2):c.4225-5G>C rs372161777
NM_002292.4(LAMB2):c.4257T>C (p.Ala1419=) rs149536828
NM_002292.4(LAMB2):c.4299G>A (p.Gly1433=) rs1165303917
NM_002292.4(LAMB2):c.4338G>A (p.Ala1446=)
NM_002292.4(LAMB2):c.4347A>C (p.Ala1449=) rs202083663
NM_002292.4(LAMB2):c.4369C>T (p.Arg1457Trp) rs151037751
NM_002292.4(LAMB2):c.4398A>G (p.Ala1466=)
NM_002292.4(LAMB2):c.4425C>T (p.Ser1475=)
NM_002292.4(LAMB2):c.460-8C>G rs200141829
NM_002292.4(LAMB2):c.4707G>A (p.Val1569=) rs1575528672
NM_002292.4(LAMB2):c.4773G>A (p.Arg1591=)
NM_002292.4(LAMB2):c.4782-15_4782-10del rs1575527834
NM_002292.4(LAMB2):c.4863C>G (p.Ala1621=)
NM_002292.4(LAMB2):c.4998C>T (p.Leu1666=) rs143723352
NM_002292.4(LAMB2):c.5061G>A (p.Thr1687=) rs150465100
NM_002292.4(LAMB2):c.5109C>T (p.Arg1703=) rs151292828
NM_002292.4(LAMB2):c.513C>T (p.Thr171=)
NM_002292.4(LAMB2):c.5142G>A (p.Lys1714=) rs139511264
NM_002292.4(LAMB2):c.5286T>C (p.Asn1762=) rs781092208
NM_002292.4(LAMB2):c.5346C>T (p.Ser1782=)
NM_002292.4(LAMB2):c.703C>T (p.Arg235Trp) rs144133177
NM_002292.4(LAMB2):c.713-7G>A rs200186640
NM_002292.4(LAMB2):c.76+10C>T rs370554848
NM_002292.4(LAMB2):c.77-9T>C
NM_002292.4(LAMB2):c.795G>A (p.Glu265=) rs375953746
NM_002292.4(LAMB2):c.816T>C (p.Tyr272=) rs151251039
NM_002292.4(LAMB2):c.915+6G>A rs2071677
NM_002292.4(LAMB2):c.951T>A (p.Arg317=) rs755050242

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