PGGT1B c.953-807A>C

Variant ID: 5-114549087-T-G

NM_005023.3(PGGT1B):c.953-807A>C

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.

Nature Communications
,
Publication Date: 2018-12-10

Variant appearance in text: rs9326953
PubMed Link: 30531953
Variant Present in the following documents:
  • 41467_2018_7524_MOESM1_ESM.pdf
View BVdb publication page