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LRRK2 c.5758-990T>G
Variant ID: 12-40727779-T-G
NM_198578.3(
LRRK2
):c.5758-990T>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.
Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03
Variant appearance in text: rs11829088
PubMed Link:
32879140
Variant Present in the following documents:
jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page
Construction and analysis of single nucleotide polymorphism-single nucleotide polymorphism interaction networks.
Iet Systems Biology
Liu, Yang Y; Li, Xutao X; Liu, Zhiping Z; Chen, Luonan L; Ng, Michael K MK
Publication Date: 2013-10
Variant appearance in text: rs11829088
PubMed Link:
24067417
Variant Present in the following documents:
Main text
View BVdb publication page
Parkinson's disease and low frequency alleles found together throughout LRRK2.
Annals Of Human Genetics
Paisán-Ruiz, Coro C; Washecka, Nicole N; Nath, Priti P; Singleton, Andrew B AB; Corder, Elizabeth H EH
Publication Date: 2009-07
Variant appearance in text: rs11829088
PubMed Link:
19489756
Variant Present in the following documents:
Main text
View BVdb publication page