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CP c.146+484T>C
Variant ID: 3-148938950-A-G
NM_000096.3(
CP
):c.146+484T>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:
Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.
Frontiers In Genetics
Pasquale, Louis R LR; Loomis, Stephanie J SJ; Aschard, Hugues H; Kang, Jae H JH; Cornelis, Marilyn C MC; Qi, Lu L; Kraft, Peter P; Hu, Frank B FB
Publication Date: 2013
Variant appearance in text: rs7652826
PubMed Link:
23386860
Variant Present in the following documents:
Main text
fgene-04-00007.pdf
View BVdb publication page