GLI3 c.1497+17766C>T

Variant ID: 7-42045301-G-A

NM_000168.5(GLI3):c.1497+17766C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of somatic chromosomal abnormalities in hypothalamic hamartoma tissue at the GLI3 locus.

American Journal Of Human Genetics
Craig, David W DW; Itty, Abraham A; Panganiban, Corrie C; Szelinger, Szabolcs S; Kruer, Michael C MC; Sekar, Aswin A; Reiman, David D; Narayanan, Vinodh V; Stephan, Dietrich A DA; Kerrigan, John F JF
Publication Date: 2008-02

Variant appearance in text: rs699487
PubMed Link: 18252217
Variant Present in the following documents:
  • Main text
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