FMR1 c.630+841T>C

Variant ID: X-147012604-T-C

NM_002024.5(FMR1):c.630+841T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Polygenic Risk Score and Risk Factors for Preeclampsia and Gestational Hypertension.

Journal Of Personalized Medicine
Perišić, Marija Majda MM; Vladimir, Klemo K; Karpov, Sarah S; Štorga, Mario M; Mostashari, Ali A; Khanin, Raya R
Publication Date: 2022-11-03

Variant appearance in text: rs29282
PubMed Link: 36579561
Variant Present in the following documents:
  • Main text
  • jpm-12-01826.pdf
View BVdb publication page



X-inactivation in female human embryonic stem cells is in a nonrandom pattern and prone to epigenetic alterations.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Shen, Yin Y; Matsuno, Youko Y; Fouse, Shaun D SD; Rao, Nagesh N; Root, Sierra S; Xu, Renhe R; Pellegrini, Matteo M; Riggs, Arthur D AD; Fan, Guoping G
Publication Date: 2008-03-25

Variant appearance in text: rs29282
PubMed Link: 18339804
Variant Present in the following documents:
  • Main text
View BVdb publication page