Bibliome.ai browser hg19
Search
About
Stats
FAQ
FRMD5 c.329+384A>G
Variant ID: 15-44211273-T-C
NM_032892.3(
FRMD5
):c.329+384A>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Common and Rare 5'UTR Variants Altering Upstream Open Reading Frames in Cardiovascular Genomics.
Frontiers In Cardiovascular Medicine
Soukarieh, Omar O; Meguerditchian, Caroline C; Proust, Carole C; Aïssi, Dylan D; Eyries, Mélanie M; Goyenvalle, Aurélie A; Trégouët, David-Alexandre DA
Publication Date: 2022
Variant appearance in text: rs492571
PubMed Link:
35387445
Variant Present in the following documents:
Main text
fcvm-09-841032.pdf
View BVdb publication page
A Mendelian randomization study of the effects of blood lipids on breast cancer risk.
Nature Communications
Nowak, Christoph C; Ärnlöv, Johan J
Publication Date: 2018-09-27
Variant appearance in text: rs492571
PubMed Link:
30262900
Variant Present in the following documents:
41467_2018_6467_MOESM1_ESM.pdf
View BVdb publication page
Role of Blood Lipids in the Development of Ischemic Stroke and its Subtypes: A Mendelian Randomization Study.
Stroke
Hindy, George G; Engström, Gunnar G; Larsson, Susanna C SC; Traylor, Matthew M; Markus, Hugh S HS; Melander, Olle O; Orho-Melander, Marju M; ,
Publication Date: 2018-04
Variant appearance in text: rs492571
PubMed Link:
29535274
Variant Present in the following documents:
str-49-820-s001.pdf
View BVdb publication page