NF1 c.7189+1174G>A

Variant ID: 17-29671327-G-A

NM_001042492.2(NF1):c.7189+1174G>A

This variant was identified in 1 publication

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: 7189+1174G>A; rs2854311
PubMed Link: 36908940
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
  • mmc2.xlsx, sheet 3
View BVdb publication page