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DSCAML1 c.511+4242C>T
Variant ID: 11-117643264-G-A
NM_020693.4(
DSCAML1
):c.511+4242C>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:
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Nature Communications
Southam, Lorraine L; Gilly, Arthur A; Süveges, Dániel D; Farmaki, Aliki-Eleni AE; Schwartzentruber, Jeremy J; Tachmazidou, Ioanna I; Matchan, Angela A; Rayner, Nigel W NW; Tsafantakis, Emmanouil E; Karaleftheri, Maria M; Xue, Yali Y; Dedoussis, George G; Zeggini, Eleftheria E
Publication Date: 2017-05-26
Variant appearance in text: rs145556679
PubMed Link:
28548082
Variant Present in the following documents:
Main text
ncomms15606-s1.pdf
ncomms15606.pdf
ncomms15606-s2.pdf
View BVdb publication page