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PAFAH1B2 c.411+711A>G
Variant ID: 11-117035319-A-G
NM_002572.3(
PAFAH1B2
):c.411+711A>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:
Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population.
Human Genomics
Moon, Sanghoon S; Lee, Young Y; Won, Sungho S; Lee, Juyoung J
Publication Date: 2018-11-01
Variant appearance in text: rs12420127
PubMed Link:
30382898
Variant Present in the following documents:
Main text
View BVdb publication page
Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians.
Journal Of Lipid Research
Gombojav, Bayasgalan B; Lee, Soo Ji SJ; Kho, Minjung M; Song, Yun-Mi YM; Lee, Kayoung K; Sung, Joohon J
Publication Date: 2016-02
Variant appearance in text: rs12420127
PubMed Link:
26634697
Variant Present in the following documents:
Main text
View BVdb publication page