Bibliome.ai browser hg19
Search
About
Stats
FAQ
CCDC155 c.1374+561G>T
Variant ID: 19-49918814-G-T
NM_144688.4(
CCDC155
):c.1374+561G>T
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:
Summary-data-based Mendelian randomization prioritizes potential druggable targets for multiple sclerosis.
Brain Communications
Jacobs, Benjamin M BM; Taylor, Thomas T; Awad, Amine A; Baker, David D; Giovanonni, Gavin G; Noyce, Alastair J AJ; Dobson, Ruth R
Publication Date: 2020
Variant appearance in text: rs1320302
PubMed Link:
33005893
Variant Present in the following documents:
Main text
fcaa119.pdf
View BVdb publication page