Bibliome.ai browser hg19
Search
About
Stats
FAQ
MTHFR c.893G>C ;(p.G298A)
Variant ID: 1-11855293-C-G
NM_005957.4(
MTHFR
):c.893G>C;(p.G298A)
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:
The β-fibrinogen gene 455G/A polymorphism associated with cardioembolic stroke in atrial fibrillation with low CHA2DS2-VaSc score.
Scientific Reports
Hu, Xiaofeng X; Wang, Junjun J; Li, Yaguo Y; Wu, Jiong J; Qiao, Song S; Xu, Shanhu S; Huang, Jun J; Chen, Linhui L
Publication Date: 2017-12-13
Variant appearance in text: MTHFR: G298A
PubMed Link:
29235504
Variant Present in the following documents:
Main text
41598_2017_Article_17537.pdf
View BVdb publication page