Gene entry
LRP2
LDL receptor related protein 2
- Chromosome
- 2
- Cytoband
- 2q31.1
- Variants (rsID)
- 104
LRP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q31.1). Its official name is “LDL receptor related protein 2”. The reference table lists 104 variants (rsID) for this gene.
Clinically classified variants
31 reference-table entries with clinical significance.
- rs115371758Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs116456291Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs143367996Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs144081819Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs145384264Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs17848169Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs188918037Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs2075252Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs2228171Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs2229263Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs2229265Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs2229266Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs34291900Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs34355135Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs34564141Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs35114151Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs375313914Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs41268685Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs4667596Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs61995915Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs79723119Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs990626Benignsingle nucleotide variantDonnai-Barrow syndrome
- rs138269726Conflicting interpretationssingle nucleotide variantDonnai-Barrow syndrome
- rs142245618Conflicting interpretationssingle nucleotide variantDonnai-Barrow syndrome
- rs144147038Conflicting interpretationssingle nucleotide variantDonnai-Barrow syndrome
- rs77686710Likely benignsingle nucleotide variantDonnai-Barrow syndrome
- rs80338747Likely pathogenicsingle nucleotide variantDonnai-Barrow syndrome
- rs111360923Uncertain significancesingle nucleotide variantDonnai-Barrow syndrome
- rs143413559Uncertain significancesingle nucleotide variantDonnai-Barrow syndrome|Inborn genetic diseases|Intellectual disability|Hearing loss and Retinal dystrophy
- rs143822500Uncertain significancesingle nucleotide variantDonnai-Barrow syndrome
- rs201115003Uncertain significancesingle nucleotide variant
Other listed variants
- rs830964
- rs830965
- rs830968
- rs830981
- rs830983
- rs831004
- rs831007
- rs831027
- rs831037
- rs2268365
- rs2268375
- rs2673177
- rs3213760
- rs3770615
- rs3770636
- rs3821126
- rs3914468
- rs4668124
- rs6759013
- rs9789747
- rs10169879
- rs10170902
- rs10198527
- rs12988804
- rs13006076
- rs16856802
- rs16856840
- rs17848152
- rs28454851
- rs41268683
- rs59363833
- rs59457398
- rs62172580
- rs71430665
- rs72874736
- rs72876246
- rs72878449
- rs72878472
- rs72878487
- rs73037817
- rs73037819
- rs74791051
- rs74846790
- rs75193630
- rs75569504
- rs76514916
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.