ClinVar Miner

List of variants reported as benign for Danon disease

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 61
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HGVS dbSNP
NM_001122606.1(LAMP2):c.*1723A>G rs142200759
NM_001122606.1(LAMP2):c.*1740A>G rs42885
NM_001122606.1(LAMP2):c.*1832C>T rs1045953
NM_001122606.1(LAMP2):c.*2199A>G rs2748
NM_001122606.1(LAMP2):c.*2209A>T rs113285013
NM_001122606.1(LAMP2):c.*409G>A rs5957380
NM_001122606.1(LAMP2):c.*410T>C rs41300908
NM_001122606.1(LAMP2):c.*848T>C rs185627568
NM_001122606.1(LAMP2):c.1094-1080C>T rs141881232
NM_001122606.1(LAMP2):c.1094-1108A>G rs73612906
NM_001122606.1(LAMP2):c.1094-1341C>G rs188897063
NM_001122606.1(LAMP2):c.1094-1383T>C rs5957381
NM_001122606.1(LAMP2):c.1094-1601T>C rs5957382
NM_001122606.1(LAMP2):c.1094-1626G>T rs2285548
NM_001122606.1(LAMP2):c.1094-173T>C rs150119198
NM_001122606.1(LAMP2):c.1094-2211A>G rs5957383
NM_001122606.1(LAMP2):c.1094-2220T>C rs750939378
NM_001122606.1(LAMP2):c.1094-237A>G rs10127182
NM_001122606.1(LAMP2):c.1094-2400A>C rs8160
NM_001122606.1(LAMP2):c.1094-2492C>T rs41300191
NM_001122606.1(LAMP2):c.1094-2664A>G rs745798436
NM_001122606.1(LAMP2):c.1094-2739T>C rs752231323
NM_001122606.1(LAMP2):c.1094-302A>G rs10127185
NM_001122606.1(LAMP2):c.1094-436A>G rs12395643
NM_001122606.1(LAMP2):c.1094-502T>C rs13441024
NM_001122606.1(LAMP2):c.1094-514T>C rs765214315
NM_001122606.1(LAMP2):c.1094-535G>A rs767123866
NM_001122606.1(LAMP2):c.1094-549A>G rs756504749
NM_001122606.1(LAMP2):c.1094-692C>G rs200014321
NM_002294.3(LAMP2):c.*1243A>G
NM_002294.3(LAMP2):c.*2518A>G
NM_002294.3(LAMP2):c.*2575G>C
NM_002294.3(LAMP2):c.*2746A>G rs3827478
NM_002294.3(LAMP2):c.*2794T>C
NM_002294.3(LAMP2):c.*3452T>C
NM_002294.3(LAMP2):c.*3459G>T
NM_002294.3(LAMP2):c.*3494A>G
NM_002294.3(LAMP2):c.*3583A>G
NM_002294.3(LAMP2):c.-32_-24GTCGCCGCC[1] rs193922648
NM_002294.3(LAMP2):c.-4G>C rs200297370
NM_002294.3(LAMP2):c.1093+2450G>A rs149783672
NM_002294.3(LAMP2):c.1093+2514G>A rs144140265
NM_002294.3(LAMP2):c.1142T>C (p.Val381Ala) rs139633545
NM_002294.3(LAMP2):c.156A>T (p.Val52=) rs12097
NM_002294.3(LAMP2):c.339C>T (p.Ser113=) rs147369153
NM_002294.3(LAMP2):c.586A>T (p.Thr196Ser) rs138991195
NM_002294.3(LAMP2):c.591G>A (p.Val197=) rs201030806
NM_002294.3(LAMP2):c.661G>A (p.Gly221Arg) rs145169006
NM_002294.3(LAMP2):c.741+11C>T rs149155417
NM_002294.3(LAMP2):c.742-16TCT[2] rs730880476
NM_002294.3(LAMP2):c.742-7_742-5del rs779710402
NM_002294.3(LAMP2):c.755T>G (p.Ile252Ser) rs141541387
NM_002294.3(LAMP2):c.927C>T (p.Ser309=) rs73219144
NM_013995.2(LAMP2):c.-33C>T rs368403767
NM_013995.2(LAMP2):c.1000G>C (p.Glu334Gln) rs766962315
NM_013995.2(LAMP2):c.157C>T (p.Arg53Cys) rs752321157
NM_013995.2(LAMP2):c.385G>A (p.Ala129Thr) rs149276836
NM_013995.2(LAMP2):c.504C>T (p.Tyr168=) rs150520869
NM_013995.2(LAMP2):c.74G>A (p.Arg25Gln) rs750118236
NM_013995.2(LAMP2):c.797G>A (p.Arg266His) rs200934351
NM_013995.2(LAMP2):c.929-5T>C rs375341409

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