MTHFR c.-14+128G>A

Variant ID: 1-11865817-C-T

NM_005957.5(MTHFR):c.-14+128G>A

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:

Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Aneji, Chiamaka N CN; Northrup, Hope H; Au, Kit Sing KS
Publication Date: 2012-02

Variant appearance in text: rs45594036
PubMed Link: 22241680
Variant Present in the following documents:
  • Main text
View BVdb publication page