NF1 c.7615+1813A>G

Variant ID: 17-29681245-A-G

NM_001042492.2(NF1):c.7615+1813A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Splicing annotation of endometrial cancer GWAS risk loci reveals potentially causal variants and supports a role for NF1 and SKAP1 as susceptibility genes.

Hgg Advances
Canson, Daffodil M DM; O'Mara, Tracy A TA; Spurdle, Amanda B AB; Glubb, Dylan M DM
Publication Date: 2023-04-13

Variant appearance in text: NF1: 7615+1813A>G; rs2525570
PubMed Link: 36908940
Variant Present in the following documents:
  • mmc2.xlsx, sheet 3
  • mmc2.xlsx, sheet 1
View BVdb publication page



A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility.

Neurogenetics
Cox, Hannah C HC; Lea, Rod A RA; Bellis, Claire C; Carless, Melanie M; Dyer, Thomas D TD; Curran, Joanne J; Charlesworth, Jac J; Macgregor, Stuart S; Nyholt, Dale D; Chasman, Daniel D; Ridker, Paul M PM; Schürks, Markus M; Blangero, John J; Griffiths, Lyn R LR
Publication Date: 2012-08

Variant appearance in text: rs2525570
PubMed Link: 22678113
Variant Present in the following documents:
  • Main text
View BVdb publication page