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HGF c.866-3492T>A
Variant ID: 7-81362587-A-T
NM_000601.4(
HGF
):c.866-3492T>A
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:
Association Analysis of Genetic Variants with Type 2 Diabetes in a Mongolian Population in China.
Journal Of Diabetes Research
Bai, Haihua H; Liu, Haiping H; Suyalatu, Suyalatu S; Guo, Xiaosen X; Chu, Shandan S; Chen, Ying Y; Lan, Tianming T; Borjigin, Burenbatu B; Orlov, Yuriy L YL; Posukh, Olga L OL; Yang, Xiuqin X; Guilan, Guilan G; Osipova, Ludmila P LP; Wu, Qizhu Q; Narisu, Narisu N
Publication Date: 2015
Variant appearance in text: rs757832
PubMed Link:
26290879
Variant Present in the following documents:
Main text
JDR2015-613236.pdf
View BVdb publication page
Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations.
Cerebrovascular Diseases (Basel, Switzerland)
Chou, S H-Y SH; Shulman, J M JM; Keenan, B T BT; Secor, E A EA; Buchman, A S AS; Schneider, J J; Bennett, D A DA; De Jager, P L PL
Publication Date: 2013
Variant appearance in text: rs757832
PubMed Link:
24135527
Variant Present in the following documents:
Main text
View BVdb publication page