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TIMD4 c.401-1266A>C
Variant ID: 5-156380067-T-G
NM_138379.2(
TIMD4
):c.401-1266A>C
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Nonparametric bounds in two-sample summary-data Mendelian randomization: Some cautionary tales for practice.
Statistics In Medicine
Trane, Ralph Møller RM; Kang, Hyunseung H
Publication Date: 2022-06-30
Variant appearance in text: rs4704727
PubMed Link:
35355302
Variant Present in the following documents:
SIM-41-2523-s001.pdf
View BVdb publication page
Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.
Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24
Variant appearance in text: rs4704727
PubMed Link:
28438747
Variant Present in the following documents:
benm033277.ww1.pdf
View BVdb publication page