ClinVar Miner

List of variants in gene LAMP2 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
Download table as spreadsheet
HGVS dbSNP
NM_001122606.1(LAMP2):c.1093+2514G>A rs144140265
NM_001122606.1(LAMP2):c.1170A>C (p.Ile390=) rs397516587
NM_001122606.1(LAMP2):c.333T>C (p.Ile111=) rs397516742
NM_001122606.1(LAMP2):c.672A>G (p.Ser224=) rs397516746
NM_001122606.1(LAMP2):c.855C>T (p.Val285=) rs397516750
NM_002294.2(LAMP2):c.*15T>C rs376806600
NM_002294.2(LAMP2):c.-23_-15delGTCGCCGCC rs193922648
NM_002294.2(LAMP2):c.-38G>C rs1354020682
NM_002294.2(LAMP2):c.1093+17C>T rs1057521759
NM_002294.2(LAMP2):c.1093+2450G>A rs149783672
NM_002294.2(LAMP2):c.1093+2589C>T rs377303143
NM_002294.2(LAMP2):c.1093+9C>G rs371259269
NM_002294.2(LAMP2):c.1094-4C>T rs768756537
NM_002294.2(LAMP2):c.1139C>T (p.Ala380Val) rs747301460
NM_002294.2(LAMP2):c.1142T>C (p.Val381Ala) rs139633545
NM_002294.2(LAMP2):c.1191T>C (p.Phe397=) rs752231323
NM_002294.2(LAMP2):c.150C>T (p.Phe50=) rs1057521701
NM_002294.2(LAMP2):c.157C>T (p.Arg53Cys) rs752321157
NM_002294.2(LAMP2):c.204C>G (p.Asp68Glu) rs376215728
NM_002294.2(LAMP2):c.276C>T (p.Phe92=) rs754577706
NM_002294.2(LAMP2):c.277G>A (p.Gly93Arg) rs727504953
NM_002294.2(LAMP2):c.299C>T (p.Ala100Val) rs397516741
NM_002294.2(LAMP2):c.339C>T (p.Ser113=) rs147369153
NM_002294.2(LAMP2):c.340G>A (p.Val114Ile) rs377652722
NM_002294.2(LAMP2):c.385G>A (p.Ala129Thr) rs149276836
NM_002294.2(LAMP2):c.398-4A>G rs1057523043
NM_002294.2(LAMP2):c.398-7T>C rs876657483
NM_002294.2(LAMP2):c.42C>T (p.Leu14=) rs727503122
NM_002294.2(LAMP2):c.504C>T (p.Tyr168=) rs150520869
NM_002294.2(LAMP2):c.517G>A (p.Val173Ile) rs141574558
NM_002294.2(LAMP2):c.586A>T (p.Thr196Ser) rs138991195
NM_002294.2(LAMP2):c.591G>A (p.Val197=) rs201030806
NM_002294.2(LAMP2):c.605A>C (p.His202Pro) rs730880475
NM_002294.2(LAMP2):c.64+16C>G rs780307352
NM_002294.2(LAMP2):c.64+20C>G rs1346805727
NM_002294.2(LAMP2):c.65-13T>A rs727503121
NM_002294.2(LAMP2):c.65-20A>T rs773064698
NM_002294.2(LAMP2):c.65-3C>T rs769801659
NM_002294.2(LAMP2):c.657A>G (p.Glu219=) rs876657484
NM_002294.2(LAMP2):c.661G>A (p.Gly221Arg) rs145169006
NM_002294.2(LAMP2):c.742-7_742-5delCCT rs779710402
NM_002294.2(LAMP2):c.755T>G (p.Ile252Ser) rs141541387
NM_002294.2(LAMP2):c.771T>C (p.Asn257=) rs138435481
NM_002294.2(LAMP2):c.813A>G (p.Leu271=) rs876657485
NM_002294.2(LAMP2):c.865-13C>T rs760238519
NM_002294.2(LAMP2):c.865-9T>C rs1057522838
NM_002294.2(LAMP2):c.877C>A (p.Arg293=) rs727503118
NM_002294.2(LAMP2):c.907A>G (p.Met303Val) rs768369360
NM_002294.2(LAMP2):c.972C>G (p.Pro324=) rs1229203142

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.