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NPC1 c.1758-968T>G
Variant ID: 18-21126081-A-C
NM_000271.4(
NPC1
):c.1758-968T>G
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:
Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework.
Nature Communications
Cho, Yoonsu Y; Haycock, Philip C PC; Sanderson, Eleanor E; Gaunt, Tom R TR; Zheng, Jie J; Morris, Andrew P AP; Davey Smith, George G; Hemani, Gibran G
Publication Date: 2020-02-21
Variant appearance in text: rs4800490
PubMed Link:
32081875
Variant Present in the following documents:
Main text
41467_2020_Article_14452.pdf
View BVdb publication page