ClinVar Miner

List of variants reported as benign for Pierson syndrome; Nephrotic syndrome, type 5, with or without ocular abnormalities by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 36
Download table as spreadsheet
HGVS dbSNP
NM_002292.4(LAMB2):c.101C>A (p.Ala34Asp) rs202057459
NM_002292.4(LAMB2):c.1193C>T (p.Thr398Ile) rs77500937
NM_002292.4(LAMB2):c.1305C>T (p.Ser435=) rs144530798
NM_002292.4(LAMB2):c.1724G>A (p.Arg575Gln) rs61729152
NM_002292.4(LAMB2):c.1764C>T (p.Pro588=) rs33942096
NM_002292.4(LAMB2):c.2095G>C (p.Gly699Arg) rs28364667
NM_002292.4(LAMB2):c.2099G>A (p.Gly700Glu) rs142860588
NM_002292.4(LAMB2):c.2307C>T (p.Leu769=) rs147076626
NM_002292.4(LAMB2):c.2505C>T (p.His835=) rs752783113
NM_002292.4(LAMB2):c.261G>A (p.Lys87=) rs149408554
NM_002292.4(LAMB2):c.2669C>T (p.Thr890Ile) rs527639885
NM_002292.4(LAMB2):c.2673C>T (p.Gly891=) rs144092322
NM_002292.4(LAMB2):c.2740G>A (p.Gly914Arg) rs35713889
NM_002292.4(LAMB2):c.2959G>A (p.Glu987Lys) rs34759087
NM_002292.4(LAMB2):c.306C>T (p.Asn102=) rs79448908
NM_002292.4(LAMB2):c.3071C>T (p.Pro1024Leu) rs368506627
NM_002292.4(LAMB2):c.3325G>A (p.Glu1109Lys) rs79677861
NM_002292.4(LAMB2):c.3387A>G (p.Gln1129=) rs34290943
NM_002292.4(LAMB2):c.3443G>A (p.Arg1148His) rs138774635
NM_002292.4(LAMB2):c.3498A>G (p.Pro1166=)
NM_002292.4(LAMB2):c.3645G>A (p.Ala1215=) rs13082063
NM_002292.4(LAMB2):c.3858G>T (p.Val1286=) rs34967349
NM_002292.4(LAMB2):c.4034G>A (p.Arg1345His) rs75073433
NM_002292.4(LAMB2):c.4163G>A (p.Arg1388Gln) rs146522641
NM_002292.4(LAMB2):c.4222C>T (p.Leu1408=) rs143974640
NM_002292.4(LAMB2):c.4370G>A (p.Arg1457Gln) rs148818522
NM_002292.4(LAMB2):c.4774C>T (p.Arg1592Trp) rs61729458
NM_002292.4(LAMB2):c.4848G>A (p.Arg1616=)
NM_002292.4(LAMB2):c.4878G>A (p.Arg1626=) rs148648480
NM_002292.4(LAMB2):c.4928A>G (p.Gln1643Arg)
NM_002292.4(LAMB2):c.5026G>A (p.Gly1676Arg) rs200747448
NM_002292.4(LAMB2):c.5027G>T (p.Gly1676Val) rs199580679
NM_002292.4(LAMB2):c.5061G>T (p.Thr1687=) rs150465100
NM_002292.4(LAMB2):c.510C>T (p.Arg170=) rs149856537
NM_002292.4(LAMB2):c.5166A>G (p.Gln1722=) rs114485284
NM_002292.4(LAMB2):c.5293G>A (p.Ala1765Thr) rs74951356

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.