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SLC38A4 c.-305+7316T>C
Variant ID: 12-47212370-A-G
NM_018018.5(
SLC38A4
):c.-305+7316T>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:
Large-scale genetic correlation scanning and causal association between deep vein thrombosis and human blood metabolites.
Scientific Reports
Luo, Pan P; Xu, Jiawen J; Cheng, Shiqiang S; Xu, Ke K; Jing, Wensen W; Zhang, Feng F; Xu, Peng P
Publication Date: 2022-05-12
Variant appearance in text: rs11183620
PubMed Link:
35551264
Variant Present in the following documents:
Main text
41598_2022_Article_12021.pdf
View BVdb publication page
Causal Inference of Carnitine on Blood Pressure and potential mediation by uric acid: A mendelian randomization analysis.
International Journal Of Cardiology. Cardiovascular Risk And Prevention
Richard, Melissa A MA; Lupo, Philip J PJ; Zachariah, Justin P JP
Publication Date: 2021-12
Variant appearance in text: rs11183620
PubMed Link:
34901954
Variant Present in the following documents:
Main text
main.pdf
View BVdb publication page