Bibliome.ai browser hg19
Search
About
Stats
FAQ
GALNT2 c.220+10307T>C
Variant ID: 1-230324364-T-C
NM_004481.3(
GALNT2
):c.220+10307T>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:
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements.
Nature Communications
Allum, Fiona F; Hedman, Åsa K ÅK; Shao, Xiaojian X; Cheung, Warren A WA; Vijay, Jinchu J; Guénard, Frédéric F; Kwan, Tony T; Simon, Marie-Michelle MM; Ge, Bing B; Moura, Cristiano C; Boulier, Elodie E; Rönnblom, Lars L; Bernatsky, Sasha S; Lathrop, Mark M; McCarthy, Mark I MI; Deloukas, Panos P; Tchernof, André A; Pastinen, Tomi T; Vohl, Marie-Claude MC; Grundberg, Elin E
Publication Date: 2019-03-14
Variant appearance in text: rs612577
PubMed Link:
30872577
Variant Present in the following documents:
41467_2019_Article_9184.pdf
View BVdb publication page