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MTHFR c.*303G>A
Variant ID: 1-11850434-C-T
NM_005957.4(
MTHFR
):c.*303G>A
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:
Minor allele of rs55763075 located in MTHFR is associated with the risk of cognitive impairment after anesthesia via modulating miR-34b.
Scientific Reports
Li, Si-Ying SY; Lei, He-Shou HS; Wu, Xiao-Yun XY; Li, Kai K; Liu, Zhi-Min ZM; Lu, Jian-Hui JH; Chen, Xiao-Yun XY
Publication Date: 2021-05-27
Variant appearance in text: rs55763075
PubMed Link:
34045473
Variant Present in the following documents:
Main text
41598_2021_Article_90229.pdf
View BVdb publication page
Genetic Landscape of Nonobstructive Azoospermia and New Perspectives for the Clinic.
Journal Of Clinical Medicine
Cerván-Martín, Miriam M; Castilla, José A JA; Palomino-Morales, Rogelio J RJ; Carmona, F David FD
Publication Date: 2020-01-21
Variant appearance in text: rs55763075
PubMed Link:
31973052
Variant Present in the following documents:
Main text
jcm-09-00300.pdf
View BVdb publication page
The SNP rs4846048 of MTHFR enhances the cervical cancer risk through association with miR-522: A preliminary report.
Molecular Genetics & Genomic Medicine
Zhou, Xinyue X; Shan, Lili L; Na, Jing J; Li, Ya Y; Wang, Jun J
Publication Date: 2020-01
Variant appearance in text: rs55763075
PubMed Link:
31750632
Variant Present in the following documents:
Main text
MGG3-8-e1055.pdf
View BVdb publication page