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LRRK2 c.7182-599T>G
Variant ID: 12-40758045-T-G
NM_198578.3(
LRRK2
):c.7182-599T>G
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Patterns of linkage disequilibrium of LRRK2 across different races: implications for genetic association studies.
Plos One
Li, Huihua H; Teo, Yik Ying YY; Tan, Eng King EK
Publication Date: 2013
Variant appearance in text: rs11835105
PubMed Link:
24040382
Variant Present in the following documents:
Main text
pone.0075041.pdf
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: rs11835105
PubMed Link:
19489756
Variant Present in the following documents:
Main text
View BVdb publication page