Bibliome.ai browser hg19
Search
About
Stats
FAQ
SORT1 c.1372-1564A>C
Variant ID: 1-109871787-T-G
NM_002959.5(
SORT1
):c.1372-1564A>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:
Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.
Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24
Variant appearance in text: rs10745352
PubMed Link:
28438747
Variant Present in the following documents:
benm033277.ww1.pdf
View BVdb publication page