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LRP1 c.67+3832G>C
Variant ID: 12-57526646-G-C
NM_002332.2(
LRP1
):c.67+3832G>C
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Common and rare variant associations with latent traits underlying depression, bipolar disorder, and schizophrenia.
Translational Psychiatry
Dattani, Saloni S; Sham, Pak C PC; Jermy, Bradley S BS; Coleman, Jonathan R I JRI; Howard, David M DM; Lewis, Cathryn M CM
Publication Date: 2023-02-06
Variant appearance in text: rs4759276
PubMed Link:
36746926
Variant Present in the following documents:
41398_2023_2324_MOESM1_ESM.pdf
View BVdb publication page