MTHFD1L c.2126-3107G>A

Variant ID: 6-151327848-G-A

NM_015440.4(MTHFD1L):c.2126-3107G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum Disorder.

Pharmaceuticals (Basel, Switzerland)
Almandil, Noor B NB; AlSulaiman, Abdulla A; Aldakeel, Sumayh A SA; Alkuroud, Deem N DN; Aljofi, Halah Egal HE; Alzahrani, Safah S; Al-Mana, Aishah A; Alfuraih, Asma A AA; Alabdali, Majed M; Alkhamis, Fahd A FA; AbdulAzeez, Sayed S; Borgio, J Francis JF
Publication Date: 2022-01-27

Variant appearance in text: rs505358
PubMed Link: 35215271
Variant Present in the following documents:
  • pharmaceuticals-15-00158.pdf
View BVdb publication page